Jump to content

User:Drsalmanshah165/Books/Medical Wikipedia 0-P

From Wikipedia, the free encyclopedia

The Wikimedia Foundation's book rendering service has been withdrawn. Please upload your Wikipedia book to one of the external rendering services.

You can still create and edit a book design using the Book Creator and upload it to an external rendering service:

MediaWiki2LaTeX provides a softcopy PDF service. Uniquely, it remains under active support and may be used online or installed locally.
Pedia Press offer final tidying and ordering of print-on-demand bound copies in (approximately) A5 format.

For help with downloading a single Wikipedia page as a PDF, see Help:Download as PDF.

This user book is a user-generated collection of Wikipedia articles that can be easily saved, rendered electronically, and ordered as a printed book. If you are the creator of this book and need help, see Help:Books (general tips) and WikiProject Wikipedia-Books (questions and assistance).

Edit this book: Book Creator · Wikitext

Order a printed copy from: PediaPress

[ About ] [ Advanced ] [ FAQ ] [ Feedback ] [ Help ] [ WikiProject ] [ Recent Changes ]

Medical Wikipedia

Abdominal aortic aneurysm

Alpha 1-antitrypsin deficiency

Alpha-1 antitrypsin deficiency panniculitis

Adhesion (medicine)

Abdominal adhesion

Abdominal cramps

Abdominal hernia

Abdominal migraine

Wolff–Parkinson–White syndrome

Radiofrequency ablation

Ablative brain surgery

Ablation of atrial fibrillation

Endometrial ablation

Late termination of pregnancy

Unsafe abortion

Abrasion (medical)

Abrasion (dental)

Abrasion (geology)

Abrasion (mechanical)

Periodontal abscess

Psychological abuse

Child sexual abuse

Paracetamol toxicity

Achilles tendon rupture

Achilles tendon

Achondroplastic dwarfism

Gastroesophageal reflux disease

List of cutaneous conditions

Acneiform eruption

Acne conglobata

Acne aestivalis

Acne keloidalis nuchae

Acne medicamentosa

Acne miliaris necrotica

Acne with facial edema

Erythrotelangiectatic rosacea

Excoriated acne

Glandular rosacea

Gram-negative rosacea

Granulomatous facial dermatitis

Perioral dermatitis

Hidradenitis suppurativa

Idiopathic facial aseptic granuloma

Lupus miliaris disseminatus faciei

Occupational acne

Periorificial dermatitis

Persistent edema of rosacea

Phymatous rosacea

Periorbital dermatitis

Pyoderma faciale

Rosacea conglobata

Steroid rosacea

Acquired brain injury

Landau–Kleffner syndrome

Acquired Epileptic Aphasia (landau-kleffner syndrome)

Actinic keratosis

Vestibular schwannoma

Acoustic neuroma

Compartment syndrome

Acute compartment syndrome

Hepatitis B virus

Acute hepatitis B

Acute intermittent porphyria

Acute kidney injury

Acute kidney failure

Acute lung injury

Acute respiratory distress syndrome

Acute lymphoblastic leukemia

Acute (medicine)

Acute lymphocytic leukemia

Acute myeloid leukemia

Acute megakaryoblastic leukemia

Acute myeloid leukemia M7

Acute pancreatitis

Acute porphyria

Addison's disease

Adenomatous polyposis coli

Gardner's syndrome

Familial adenomatous polyposis

Adenoid cystic carcinoma

Adenoid squamous-cell carcinoma

Squamous-cell carcinoma

Adenoid hypertrophy

Adenoid basal cell carcinoma

Basal-cell carcinoma

Adenoid seborrheic keratosis

Reticulated seborrheic keratosis

Adenovirus infection

Adrenal insufficiency

Adult Brain Tumor

Adult-onset diabetes

Diabetes mellitus type 2

Adult-onset Still's disease

Adult stem cell

Patient Protection and Affordable Care Act

Affordable Care Act

Alpha-fetoprotein

Hirschsprung's disease

Age-related macular degeneration

Macular degeneration

Agranulocytosis

Airsickness bag

Aminolevulinic acid dehydratase deficiency porphyria

Alcohol withdrawal syndrome

Alcohol dependence

Alcohol dependence syndrome

Alcohol intoxication

Alcohol poisoning

Allergic asthma

Allergic conjunctivitis

Allergic granulomatosis

Churg–Strauss syndrome

Allergic rhinitis

Henoch–Schönlein purpura

Allergic purpura

Allergic reaction

Allergic reactions to anaesthesia

Allergen immunotherapy

Alopecia areata

Alopecia areata universalis

Alopecia universalis

Alopecia areata totalis

Alopecia totalis

Alpha-thalassemia

Alpha-thalassemia mental retardation syndrome

Alpha-1 proteinase inhibitor

Alpha-1 related emphysema

Alpha-galactosidase

Alpha-galactosidase A deficiency

Alport syndrome

Amyotrophic lateral sclerosis

Alanine transaminase

Alveolar osteitis

Alzheimer's disease

Antimitochondrial antibody

Anti-mitochondrial antibody

American trypanosomiasis

Irritant diaper dermatitis

Amyloidosis, familial

Antinuclear antibody

Anti-nuclear antibody

Anaphylactoid purpura

List of diseases (A)

Aagenaes syndrome

Aarskog–Scott syndrome

Abdallat–Davis–Farrage syndrome

Abdominal wall defect

Abdominal musculature absent with microphthalmia and joint laxity

Aberrant subclavian artery

Ablepharon macrostomia syndrome

Abruzzo–Erickson syndrome

Absence of gluteal muscle

Lymphocytopenia

Acanthocheilonemiasis

Chorea acanthocytosis

Acanthosis nigricans

Accessory navicular bone

Accessory pancreas

Triple-A syndrome

Achard syndrome

Achard–Thiers syndrome

Achondrogenesis

Achondrogenesis type 1B

Achondrogenesis type 2

Glycogen storage disease type II

Isovaleric acidemia

Propionic acidemia

Ackerman syndrome

Ichthyosis acquisita

Acrofrontofacionasal dysostosis

Acrocallosal syndrome

Acrodermatitis enteropathica

Nager acrofacial dysostosis

Acrokeratoelastoidosis of Costa

Acromicric dysplasia

Acropectoral syndrome

Adrenocorticotropic hormone deficiency

Glucocorticoid deficiency 1

Activated protein C resistance

Febrile neutrophilic dermatosis

Guillain–Barré syndrome

Acute monocytic leukemia

Altitude sickness

Acute myeloblastic leukemia

Minimally differentiated acute myeloblastic leukemia

Acute myeloblastic leukemia with maturation

Acute myeloblastic leukemia without maturation

Acute myelomonocytic leukemia

Acute necrotizing ulcerative gingivitis

Acute posterior multifocal placoid pigment epitheliopathy

Acute promyelocytic leukemia

Acute tubular necrosis

Medium-chain acyl-coenzyme A dehydrogenase deficiency

Short-chain acyl-coenzyme A dehydrogenase deficiency

Very long-chain acyl-coenzyme A dehydrogenase deficiency

Amniotic band constriction

Adams–Nance syndrome

Adams–Oliver syndrome

Adducted thumb syndrome

Adenine phosphoribosyltransferase deficiency

Adenocarcinoma of the lung

Adenosine deaminase deficiency

Adenosine Monophosphate Deaminase Deficiency type 1

Adenylosuccinate lyase deficiency

Adiposis dolorosa

Adrenal gland disorder

Adrenocortical hyperfunction

Congenital adrenal hyperplasia

X-linked adrenal hypoplasia congenita

Adrenocortical carcinoma

Adrenoleukodystrophy

Muscular dystrophy

Adult attention deficit hyperactivity disorder

Spinal muscular atrophy

Advanced sleep phase disorder

African trypanosomiasis

Congenital afibrinogenemia

Aggressive fibromatosis

Hyperprolactinaemia

Aicardi syndrome

Aicardi–Goutières syndrome

HIV-associated neurocognitive disorder

Alagille syndrome

Albinism–deafness syndrome

Chédiak–Higashi syndrome

Albright's hereditary osteodystrophy

McCune–Albright syndrome

Fetal alcohol syndrome

Alcoholic hepatitis

Aldolase A deficiency

Allan–Herndon–Dudley syndrome

Allergic bronchopulmonary aspergillosis

Alopecia contractures dwarfism mental retardation

Alpers' disease

Alpha-mannosidosis

Alström syndrome

Alternating hemiplegia

Alternating hemiplegia of childhood

Alveolar capillary dysplasia

Alveolar hydatid disease

Alveolar soft part sarcoma

Hypersensitivity pneumonitis

Early-onset Alzheimer's disease

Leber's congenital amaurosis

Amelia (birth defect)

Yim–Ebbin syndrome

Amelogenesis imperfecta

Anterograde amnesia

Childhood amnesia

Psychogenic amnesia

Drug-induced amnesia

Lacunar amnesia

Retrograde amnesia

Transient global amnesia

Anaplastic thyroid cancer

Androgen insensitivity syndrome

Diamond–Blackfan anemia

Congenital hypoplastic anemia

Sideroblastic anemia

Aneurysm of sinus of Valsalva

Intracranial aneurysm

Angioimmunoblastic T-cell lymphoma

Angiostrongyliasis

Strongyloidiasis

Aniridia ataxia renal agenesis psychomotor retardation

Ankylosing spondylitis

Annular pancreas

Annuloaortic ectasia

Imperforate anus

Anorexia nervosa

Anterior horn disease

Antiphospholipid syndrome

Antisocial personality disorder

Antisynthetase syndrome

Antley–Bixler syndrome

Anton–Babinski syndrome

Aortic aneurysm

Interrupted aortic arch

Coarctation of the aorta

Aortic dissection

Aortic valve stenosis

Aphthous stomatitis

Aplasia cutis congenita

Aplastic anemia

Reticulocytopenia

Apparent mineralocorticoid excess syndrome

Roberts syndrome

Aqueductal stenosis

Arakawa's syndrome II

Arthrogryposis–renal dysfunction–cholestasis syndrome

Argentine hemorrhagic fever

AREDYLD syndrome

Argininosuccinic aciduria

Arnold–Chiari malformation

Aromatase deficiency

Aromatase excess syndrome

Arrhythmogenic right ventricular dysplasia

Arsenic poisoning

Arterial tortuosity syndrome

Arteriovenous malformation

Juvenile idiopathic arthritis

Metachromatic leukodystrophy

Ascher's syndrome

Aseptic meningitis

Asherman's syndrome

Ashman phenomenon

Aspartylglucosaminuria

Asperger syndrome

Perinatal asphyxia

Astigmatism (eye)

Hypertrophic cardiomyopathy

Ataxia telangiectasia

Atelosteogenesis, type II

Atherosclerosis

Atopic dermatitis

Intestinal atresia

Atrioventricular fistula

Atrioventricular septal defect

Atrial septal defect

Atrophic vaginitis

Attention deficit hyperactivity disorder

Auditory processing disorder

Autoimmune hemolytic anemia

Autoimmune hepatitis

Autoimmune polyendocrine syndrome

Avoidant personality disorder

Peripheral neuropathy

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

Distal Trisomy 10q

Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency

17-beta-hydroxysteroid dehydrogenase deficiency

17q21.31 microdeletion syndrome

1p36 deletion syndrome

2-Hydroxyglutaric aciduria

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

DiGeorge syndrome

Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency

3 hydroxyisobutyric aciduria

3-Methylcrotonyl-CoA carboxylase deficiency

3-hydroxy-3-methylglutaryl-CoA lyase deficiency

3-hydroxyacyl-coenzyme A dehydrogenase deficiency

3-Methylglutaconic aciduria

Optic neuropathy

XX gonadal dysgenesis

Klinefelter syndrome

Triple X syndrome

49, XXXXY syndrome

5-alpha-reductase deficiency

Chromosome 5q deletion syndrome

6-Pyruvoyltetrahydropterin synthase deficiency

Smith–Lemli–Opitz syndrome

8p23.1 duplication syndrome

9q34 deletion syndrome

Bacillus cereus

Foodborne illness

Gastroenteritis

Bacterial pneumonia

Bacterial vaginosis

Auditory brainstem response

Infective endocarditis

Neurofibromatosis type II

Bangstad syndrome

Bannayan–Riley–Ruvalcaba syndrome

African iron overload

Banti's syndrome

Barbiturate dependence

Barbiturate overdose

Bardet–Biedl syndrome

Bare lymphocyte syndrome

Barrett's esophagus

Bare lymphocyte syndrome 2

Multiple pterygium syndrome

Bartter syndrome

Basal ganglia disease

Bazex–Dupré–Christol syndrome

Congenital contractural arachnodactyly

Myotonia congenita

Becker's muscular dystrophy

Short rib – polydactyly syndrome

Behçet's disease

Nonvenereal endemic syphilis

Pilocytic astrocytoma

Essential tremor

Thin basement membrane disease

Benign fasciculation syndrome

Cicatricial pemphigoid

Benign paroxysmal positional vertigo

Benzodiazepine dependence

Benzodiazepine overdose

Benzodiazepine withdrawal syndrome

Congenital generalized lipodystrophy

Berdon syndrome

IgA nephropathy

Nijmegen breakage syndrome

Beta-ketothiolase deficiency

Beta-mannosidosis

Beta thalassemia

Promoter (genetics)

Bethlem myopathy

Bhaskar–Jagannathan syndrome

Glycogen storage disease type XI

Bicuspid aortic valve

Biemond syndrome

Potter sequence

Biliary atresia

Primary biliary cirrhosis

Cholangiocarcinoma

Binswanger's disease

Bipolar disorder

Bipolar I disorder

Bipolar II disorder

Biotin deficiency

Biotinidase deficiency

Birdshot chorioretinopathy

Birt–Hogg–Dubé syndrome

Björnstad syndrome

Pashayan syndrome

Blepharophimosis

Blount's disease

Blue diaper syndrome

Blue rubber bleb nevus syndrome

Body dysmorphic disorder

Bolivian hemorrhagic fever

Osteogenesis imperfecta

Bone marrow failure

Turner syndrome

Boomerang dysplasia

Borderline personality disorder

Tuberous sclerosis

Bowen's disease

Bowenoid papulosis

Diphyllobothrium

Cornelia de Lange Syndrome

Cavernous hemangioma

Branchio-oculo-facial syndrome

Branchio-oto-renal syndrome

Brazilian hemorrhagic fever

Hereditary breast–ovarian cancer syndrome

Brief psychotic disorder

Bright's disease

Familial dysbetalipoproteinemia

Olfactory reference syndrome

Bronchiolitis obliterans organizing pneumonia

Bronchopulmonary dysplasia

Brown's syndrome

Brown-Séquard syndrome

X-linked agammaglobulinemia

Budd–Chiari syndrome

Thromboangiitis obliterans

Bulimia nervosa

Bullous pemphigoid

Burkitt's lymphoma

Burning mouth syndrome

Buschke–Ollendorff syndrome

Medullary sponge kidney

Café au lait spot

Caffeine-induced sleep disorder

Infantile cortical hyperostosis

Calculus (medicine)

Calcinosis cutis

CAMFAK syndrome

Campylobacteriosis

Camurati–Engelmann disease

Canavan disease

Canine distemper

Cannabis dependence

Effects of cannabis

Canga's bead symptom

Caplan's syndrome

Ornithine translocase deficiency

Congenital disorder of glycosylation

Carcinoid syndrome

Cardiac amyloidosis

Cardiac tamponade

Cardiofaciocutaneous syndrome

Dilated cardiomyopathy

Restrictive cardiomyopathy

Caregiver syndrome

Systemic primary carnitine deficiency

Carnitine palmitoyltransferase I deficiency

Carnitine palmitoyltransferase II deficiency

Carnitine-acylcarnitine translocase deficiency

Carotid artery dissection

Carpal tunnel syndrome

Carpenter syndrome

Eosinophilic pneumonia

Cartilage–hair hypoplasia

Castleman's disease

Cat eye syndrome

Cat scratch disease

Congenital cataract

Catel–Manzke syndrome

Caudal regression syndrome

Complex regional pain syndrome

Cavernous sinus thrombosis

Asymmetric crying facies

Gluten-sensitive enteropathy-associated conditions

Coeliac disease

Cenani–Lenz syndactylism

Central core disease

Neurogenic diabetes insipidus

Central serous retinopathy

Centronuclear myopathy

Cerebellar hypoplasia

Cerebral amyloid angiopathy

CADASIL syndrome

Cerebral hypoxia

Ventricular system

Cockayne syndrome

Neuronal ceroid lipofuscinosis

Cervical cancer

Spinal stenosis

Klippel–Feil syndrome

Neutral lipid storage disease

Iridocorneal endothelial syndrome

Charcot disease

Charcot–Marie–Tooth disease

CHARGE syndrome

Fahr's syndrome

Ho–Kaufman–Mcalister syndrome

Childhood disintegrative disorder

Chimera (genetics)

Glutamate flavoring

Chlamydia trachomatis

Chlamydia infection

Chlamydophila pneumoniae

Primary sclerosing cholangitis

Progressive familial intrahepatic cholestasis

Cholesteryl ester storage disease

Lipid pneumonia

Chondroblastoma

Chondrocalcinosis

X-linked recessive chondrodysplasia punctata

Chondrodysplasia punctata

Chondrodystrophy

Ellis–van Creveld syndrome

Chondromalacia patellae

Sydenham's chorea

Paroxysmal nonkinesigenic dyskinesia

Choriocarcinoma

Chorioretinitis

Choroid plexus cyst

Choroid plexus papilloma

Chromoblastomycosis

Renal cell carcinoma

Chromosome 15q partial deletion

Chromosome 15q trisomy

Edwards syndrome

Ring chromosome 20 syndrome

Chronic obstructive pulmonary disease

Chronic fatigue syndrome

Chronic granulomatous disease

Chronic inflammatory demyelinating polyneuropathy

B-cell chronic lymphocytic leukemia

Chronic mountain sickness

Chronic myelogenous leukemia

Chronic myelomonocytic leukemia

Polyradiculoneuropathy

Chronic recurrent multifocal osteomyelitis

Chronic kidney disease

Spasmodic dysphonia

Neonatal onset multisystem inflammatory disease

Capillary leak syndrome

Cleft lip and palate

Cleidocranial dysostosis

Cloacal exstrophy

Clouston's hidrotic ectodermal dysplasia

Cluster headache

Cytomegalovirus

Coalworker's pneumoconiosis

Cocaine dependence

Cocaine intoxication

Coccidioidomycosis

Coffin–Lowry syndrome

Coffin–Siris syndrome

Cold agglutinin disease

Cold antibody hemolytic anemia

Connective tissue disease

Collagenous colitis

Hereditary nonpolyposis colorectal cancer

Color blindness

Colorado tick fever

Combined hyperlipidemia

Common variable immunodeficiency

Complement component 2

Complement receptor 1

Conduct disorder

Conductive hearing loss

Condylomata lata

Lipoid congenital adrenal hyperplasia

Congenital amputation

Congenital pulmonary airway malformation

Congenital diaphragmatic hernia

Congenital dyserythropoietic anemia

Gunther disease

Möbius syndrome

Congenital fiber type disproportion

Infantile myofibromatosis

Congenital heart defect

Congenital hemolytic anemia

Congenital hepatic fibrosis

Herpes simplex virus

Congenital hypothyroidism

Congenital ichthyosiform erythroderma

Congenital insensitivity to pain with anhidrosis

Mesoblastic nephroma

Microvillous inclusion disease

Mitral valve stenosis

Congenital myopathy

Congenital nephrotic syndrome

Congenital rubella syndrome

Hereditary spherocytosis

Congenital syphilis

Conn's syndrome

Conradi–Hünermann syndrome

Constitutional growth delay

Bronchiolitis obliterans

Contact dermatitis

Allergic contact dermatitis

Irritant contact dermatitis

Conversion disorder

Cor triatriatum

Corneal dystrophy

Corneodermatoosseous syndrome

Coronary artery aneurysm

Coronary artery disease

Agenesis of the corpus callosum

Cortical dysplasia

Corticobasal degeneration

Costello syndrome

Costochondritis

Tietze syndrome

Robinow syndrome

Cowden syndrome

Cramp fasciculation syndrome

Crandall syndrome

Craniodiaphyseal dysplasia

Crouzon syndrome

Craniofrontonasal dysplasia

Craniosynostosis

Creutzfeldt–Jakob disease

Crigler–Najjar syndrome

Crohn's disease

Cronkhite–Canada syndrome

Crouzonodermoskeletal syndrome

Cryoglobulinemia

Cryptosporidiosis

Crystal arthropathy

Currarino syndrome

Cushing's syndrome

Cutaneous larva migrans

Lupus erythematosus

Cutaneous T cell lymphoma

Cutaneous small-vessel vasculitis

De Barsy syndrome

Cutis marmorata telangiectatica congenita

Cutis verticis gyrata

Cyclic neutropenia

Cyclic vomiting syndrome

Cystic fibrosis

Cytochrome c oxidase

Daentl Towsend Siegel syndrome

Dahlberg Borer Newcomer syndrome

Dandy–Walker syndrome

Darier's disease

DeSanctis–Cacchione syndrome

Peeling skin syndrome

Deep vein thrombosis

Dejerine–Sottas disease

Delayed ejaculation

Delayed sleep phase disorder

Delirium tremens

Delusional disorder

Oculocerebrocutaneous syndrome

Familial British dementia

Frontotemporal dementia

Alcohol-related dementia

Dementia pugilistica

Vascular dementia

Dementia with Lewy bodies

Demyelinating disease

Dental fluorosis

Dentatorubral-pallidoluysian atrophy

Dentin dysplasia

Dentinogenesis imperfecta

Dependent personality disorder

Depersonalization disorder

Major depressive disorder

Depressive personality disorder

Ectodermal dysplasia

Dermatitis herpetiformis

Dermatographic urticaria

Benign fibrous histiocytoma

Dermatomyositis

Dermatopathia pigmentosa reticularis

Dermatophytosis

Dermoodontodysplasia

Larsen syndrome

Desmin-related myofibrillar myopathy

Desmoplastic small-round-cell tumor

Developmental coordination disorder

Neuromyelitis optica

D-Glyceric acidemia

Diabetes insipidus

Nephrogenic diabetes insipidus

Diabetes mellitus

Diabetes mellitus type 1

Diabetic angiopathy

Diabetic nephropathy

Diabetic neuropathy

Diastematomyelia

Diastrophic dysplasia

Lysinuric protein intolerance

Dicarboxylic aminoaciduria

Diethylstilbestrol

Diffuse idiopathic skeletal hyperostosis

Diffuse neonatal hemangiomatosis

Diffuse panbronchiolitis

Interstitial lung disease

Digoxin toxicity

Dihydropyrimidine dehydrogenase deficiency

Discoid lupus erythematosus

Disinhibited attachment disorder

Perifolliculitis capitis abscedens et suffodiens

Dissociative disorder

Dissociative identity disorder

Distal muscular dystrophy

Ichthyosis vulgaris

Donnai–Barrow syndrome

Dopamine beta hydroxylase deficiency

Transposition of the great vessels

Double outlet right ventricle

Dubowitz syndrome

Duchenne muscular dystrophy

Dubin–Johnson syndrome

Duodenal atresia

Dupuytren's contracture

Occupational lung disease

Dyschromatosis universalis hereditaria

Meckel syndrome

VLDLR-associated cerebellar hypoplasia

Congenital dyserythropoietic anemia type I

Congenital dyserythropoietic anemia type II

Congenital dyserythropoietic anemia type III

Dysferlinopathy

Dysfibrinogenemia

Dyskeratosis congenita

Tardive dyskinesia

Dysplastic nevus syndrome

Myotonic dystrophy

Epidermolysis bullosa dystrophica

Ebola virus disease

Ectopic pregnancy

Ectrodactyly–ectodermal dysplasia–cleft syndrome

Ehlers–Danlos syndrome

Eisenmenger's syndrome

Elective mutism

Elejalde syndrome

Proteus syndrome

Emery–Dreifuss muscular dystrophy

Empty sella syndrome

Encephalitis lethargica

Encephalomyelitis

Sturge–Weber syndrome

Enchondromatosis

Endocardial fibroelastosis

Endometrial stromal sarcoma

Hypereosinophilic syndrome

Enolase deficiency

Entomophthoramycosis

Bothrops lanceolatus

Eosinophilia–myalgia syndrome

Eosinophilic cystitis

Eosinophilic fasciitis

Eosinophilic gastroenteritis

Eosinophilic granuloma

Eosinophilic folliculitis

Fear of daylight

Primitive neuroectodermal tumor

Epidermodysplasia verruciformis

Epidermolysis bullosa acquisita

Junctional epidermolysis bullosa (medicine)

Epidermolysis bullosa

Epidermolytic hyperkeratosis

Epilepsia partialis continua

Benign familial neonatal seizures

Absence seizure

Progressive myoclonus epilepsy

Galactose epimerase deficiency

Pacman dysplasia

Epithelial-myoepithelial carcinoma

Erythropoietic protoporphyria

Infectious mononucleosis

Erdheim–Chester disease

Erosive pustular dermatitis of the scalp

Erythema multiforme

Erythema nodosum

Erythromelalgia

Erythroblastopenia

Erythrokeratodermia with ataxia

Erythrokeratodermia variabilis

Keratolytic winter erythema

Erythroplasia of Queyrat

Pathogenic Escherichia coli

Esophageal atresia

Esophageal cancer

Esophageal varices

Essential fatty acid

Essential hypertension

Thrombocytopenia

Essential thrombocythaemia

Esthesioneuroblastoma

Organic acidemia

Ewing's sarcoma

Serpentine fibula-polycystic kidney syndrome

Hereditary multiple exostoses

Experimental autoimmune encephalomyelitis

Exploding head syndrome

Bladder exstrophy

Movement disorder

Seaver Cassidy syndrome

Facial nerve paralysis

Facioscapulohumeral muscular dystrophy

Factor V Leiden

Factor XIII deficiency

Multiple epiphyseal dysplasia

Tetralogy of Fallot

Transthyretin-related hereditary amyloidosis

Familial aortic dissection

Colorectal cancer

Familial dysautonomia

Lipoprotein lipase deficiency

Familial hypertriglyceridemia

Hypopituitarism

Familial Mediterranean fever

Periodic paralysis

Treacher Collins syndrome

Catecholaminergic polymorphic ventricular tachycardia

Fanconi syndrome

Fatal familial insomnia

Fazio–Londe disease

Febrile seizure

Fechtner syndrome

Feingold syndrome

Felty's syndrome

Female sexual arousal disorder

Femur fibula ulna syndrome

Congenital cytomegalovirus infection

Fetal hydantoin syndrome

Hydrops fetalis

Fetal warfarin syndrome

Fibrochondrogenesis

Fibromuscular dysplasia

Idiopathic pulmonary fibrosis

Fibrous dysplasia of bone

Fibrodysplasia ossificans progressiva

Lattice corneal dystrophy

Fish-eye disease

Fissured tongue

Fitz-Hugh–Curtis syndrome

Fitzsimmons–Guilbert syndrome

Pseudomonas oryzihabitans

Necrotizing fasciitis

Floating-Harbor syndrome

Endosalpingiosis

Flynn–Aird syndrome

Focal dermal hypoplasia

Focal facial dermal dysplasia

Foix–Chavany–Marie syndrome

Foix–Alajouanine syndrome

Follicular lymphoma

Glycogen storage disease type III

Foreign accent syndrome

Fountain syndrome

Fournier gangrene

Fox–Fordyce disease

Fragile X syndrome

Franceschetti–Klein syndrome

Hallermann–Streiff syndrome

Fraser syndrome

Frasier syndrome

Infantile free sialic acid storage disease

Freeman–Sheldon syndrome

Freiberg disease

Frey's syndrome

Friedreich's ataxia

Adiposogenital dystrophy

Frontonasal dysplasia

Hereditary fructose intolerance

Fructose 1,6-bisphosphatase

Essential fructosuria

Fukuyama congenital muscular dystrophy

Fumarase deficiency

Neuroendocrine tumor

List of diseases (G)

Galactokinase deficiency

Galactorrhea hyperprolactinemia

Morquio syndrome

Galactose-1-phosphate uridylyltransferase deficiency

Galloway Mowat syndrome

Hyperkalemic periodic paralysis

GM2 gangliosidoses

GM1 gangliosidoses

Ganser syndrome

Painful bruising syndrome

Nissen fundoplication

Gastric dumping syndrome

Gastric lymphoma

Gastrocutaneous syndrome

Gastrointestinal cancer

Gaucher's disease

Weill–Marchesani syndrome

Gender identity disorder

Miller syndrome

Generalized anxiety disorder

Thyroid hormone resistance

Generalised epilepsy

Koro (medicine)

Geographic tongue

Fetal trimethadione syndrome

Gerodermia osteodysplastica

Gerstmann syndrome

Gestational diabetes

Gestational pemphigoid

Gestational trophoblastic disease

Gianotti–Crosti syndrome

Giant axonal neuropathy

Giant-cell arteritis

Idiopathic giant-cell myocarditis

Congenital melanocytic nevus

Giant platelet disorder

Gilbert's syndrome

Tourette syndrome

Gitelman syndrome

Glanzmann's thrombasthenia

Glioblastoma multiforme

Gliomatosis cerebri

Glomerulonephritis

Glomerulosclerosis

Glucose-6-phosphate dehydrogenase deficiency

Glucose-galactose malabsorption

Glutaric aciduria type 1

Glutathione synthetase deficiency

Glycogen storage disease

Glycogen storage disease type I

Glycogen storage disease type VI

Phosphofructokinase deficiency

Glycogen storage disease type V

Glycogen storage disease type IV

Glycogen storage disease type 0

Goldenhar syndrome

Gonadal dysgenesis

Mixed gonadal dysgenesis

XY gonadal dysgenesis

Neisseria gonorrhoeae

Goodpasture syndrome

Gorham's disease

Gougerot–Blum syndrome

Graft-versus-host disease

Granuloma annulare

Lymphomatoid granulomatosis

Graves' disease

Gray platelet syndrome

Hydrops-ectopic calcification-moth-eaten skeletal dysplasia

Transient acantholytic dermatosis

Growth hormone deficiency

Guanidinoacetate methyltransferase deficiency

Hagemoser–Weinstein–Bresnick syndrome

Hailey–Hailey disease

Hairy cell leukemia

Hairy palms and soles

Black hairy tongue

Hajdu–Cheney syndrome

Pantothenate kinase-associated neurodegeneration

Hallucinogen persisting perception disorder

Nevus sebaceous

Hand, foot and mouth disease

Hand–Schüller–Christian disease

Tyrosinemia type II

Harlequin-type ichthyosis

Hartnup disease

Hashimoto's thyroiditis

Congenital self-healing reticulohistiocytosis

Hay–Wells syndrome

Aneurysm of heart

Myocardial infarction

Primary tumors of the heart

Heavy metal (chemistry)

Hemangioblastoma

Hemangioendothelioma

Kasabach–Merritt syndrome

Hemangiopericytoma

Hemifacial microsomia

Familial hemiplegic migraine

HFE hereditary haemochromatosis

Juvenile hemochromatosis

Haemochromatosis type 3

Hemoglobinopathy

Hemolytic-uremic syndrome

Hemophagocytic lymphohistiocytosis

Hantavirus hemorrhagic fever with renal syndrome

Bernard–Soulier syndrome

Hennekam syndrome

Heparin-induced thrombocytopenia

Hepatic encephalopathy

Hepatic veno-occlusive disease

Hepatocellular carcinoma

Hepatorenal syndrome

Type I tyrosinemia

Hereditary angioedema

Hereditary coproporphyria

Hereditary elliptocytosis

Hereditary hemorrhagic telangiectasia

Methemoglobinemia

Hereditary pancreatitis

Hereditary spastic paraplegia

Hermansky–Pudlak syndrome

Herpesviral encephalitis

Neonatal herpes simplex

Ramsay Hunt syndrome type II

Herpes of the eye

TNF receptor associated periodic syndrome

Sprengel's deformity

Dislocation of hip

Hip dysplasia (canine)

Hip dysplasia (human)

Junctional ectopic tachycardia

Orthomolecular medicine

Langerhans cell histiocytosis

Non-Langerhans cell histiocytosis

Histrionic personality disorder

Hodgkin's lymphoma

Smith–Fineman–Myers syndrome

Holocarboxylase synthetase deficiency

Holoprosencephaly

Holt–Oram syndrome

Horner's syndrome

Horseshoe kidney

Hot tub folliculitis

Howel–Evans syndrome

Ehrlichiosis ewingii infection

Human granulocytic anaplasmosis

Human monocytotropic ehrlichiosis

Hunter syndrome

Huntington's disease

Hurler syndrome

Hutchinson's teeth

Molar pregnancy

Hydranencephaly

Hydrolethalus syndrome

Primary hyperoxaluria

Hyperimmunoglobulin E syndrome

Hyper IgM syndrome

Hyperaldosteronism

Hyperandrogenism

Hypercementosis

Hypercholesterolemia

Hyperglycerolemia

Hyperglycinemia

Hyperhomocysteinemia

Hyper-IgD syndrome

Congenital hyperinsulinism

Hyperostosis frontalis interna

Hyperparathyroidism

Hyperphenylalaninemia

Pipecolic acidemia

Hyperprolinemia

Hypersensitivity

Type I hypersensitivity

Type II hypersensitivity

Type III hypersensitivity

Type IV hypersensitivity

Hypertensive retinopathy

Hyperthyroidism

Hypertriglyceridemia

Hypertryptophanemia

Hypervitaminosis A

Hypervitaminosis D

Hypervitaminosis E

Hypoactive sexual desire disorder

Hypoaldosteronism

Hypobetalipoproteinemia

Hypochondriasis

Hypochondrogenesis

Hypochondroplasia

Urticarial vasculitis

Hypohidrotic ectodermal dysplasia

Hypokalemic periodic paralysis

Hypokalemic sensory overstimulation

Hypolipoproteinemia

Prader–Willi syndrome

Hypoparathyroidism

Hypophosphatasia

X-linked hypophosphatemia

Hypoplastic left heart syndrome

Michels Caskey syndrome

Hypoprothrombinemia

Pallister–Hall syndrome

Tuber cinereum hamartoma

Hypoxia (medical)

Trichothiodystrophy

Immunodeficiency–centromeric instability–facial anomalies syndrome

Ichthyoallyeinotoxism

Ichthyosis bullosa of Siemens

Ruzicka Goerz Anton syndrome

Ichthyosis follicularis with alopecia and photophobia syndrome

Ichthyosis linearis circumflexa

Netherton syndrome

Juvenile osteoporosis

Idiopathic pulmonary haemosiderosis

Idiopathic sclerosing mesenteritis

Idiopathic thrombocytopenic purpura

Selective immunoglobulin A deficiency

Iminoglycinuria

Impossible syndrome

Inborn error of metabolism

Inborn errors of renal tubular transport

Urea cycle disorder

Incontinentia pigmenti

Incontinentia pigmenti achromians

Infant respiratory distress syndrome

Infantile digital fibromatosis

Epileptic spasms

Spinal muscular atrophies

Septic arthritis

Inflammatory breast cancer

Inguinal hernia

Intoxicative inhalant

Intraocular lymphoma

Interstitial cystitis

Whipple's disease

Intestinal pseudoobstruction

Intestinal spirochetosis

Cerebral arteriovenous malformation

Vertically transmitted infection

Iodine deficiency

Iridogoniodysgenesis, dominant type

Iron deficiency

Irritable bowel syndrome

Asplenia with cardiovascular anomalies

Jackson–Weiss syndrome

Jacobsen syndrome

Pachyonychia congenita

Jalili syndrome

Spinal muscular atrophy with progressive myoclonic epilepsy

Jansky–Bielschowsky disease

Japanese encephalitis

Spondylocostal dysostosis

Jervell and Lange-Nielsen syndrome

Asphyxiating thoracic dysplasia

Johanson–Blizzard syndrome

Johnson–Munson syndrome

Joubert syndrome

Jumping Frenchmen of Maine

Juvenile dermatomyositis

Lesch–Nyhan syndrome

Juvenile hyaline fibromatosis

Juvenile myoclonic epilepsy

Kabuki syndrome

Kallmann syndrome

Kaposi's sarcoma

Kapur–Toriello syndrome

Primary ciliary dyskinesia

Kaufman oculocerebrofacial syndrome

Kawasaki disease

Kearns–Sayre syndrome

Spinal and bulbar muscular atrophy

Keratoacanthoma

Keratoconjunctivitis sicca

Keratosis follicularis spinulosa decalvans

Keratosis pilaris

Seborrheic keratosis

Keutel syndrome

Anaplastic large-cell lymphoma

Keratitis–ichthyosis–deafness syndrome

Kikuchi disease

Kimura's disease

Malignant hyperthermia

Kjer's optic neuropathy

Kleine–Levin syndrome

Klippel–Trénaunay syndrome

Klumpke paralysis

Klüver–Bucy syndrome

Kniest dysplasia

Familial partial lipodystrophy

Kocher–Debre–Semelaigne syndrome

Köhler disease

Kohlschütter-Tönz syndrome

Korsakoff's syndrome

Kostmann syndrome

Kowarski syndrome

Peters-plus syndrome

Kyasanur forest disease

Lachiewicz–Sibley syndrome

Lambert–Eaton myasthenic syndrome

Lamellar ichthyosis

John Langdon Down

Langer–Giedion syndrome

Diffuse large B-cell lymphoma

Laryngeal cancer

Laryngeal cleft

Laryngeal papillomatosis

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Leber's hereditary optic neuropathy

Lecithin cholesterol acyltransferase deficiency

Plantar fibromatosis

Left ventricular hypertrophy

Legg–Calvé–Perthes syndrome

Legionnaires' disease

Leigh's disease

Leiner's disease

Lemierre's syndrome

Lennox–Gastaut syndrome

Lenz microphthalmia syndrome

Donohue syndrome

Leri pleonosteosis

Léri–Weill dyschondrosteosis

Lethal congenital contracture syndrome

Letterer–Siwe disease

Maple syrup urine disease

Myeloid leukemia

T-cell prolymphocytic leukemia

Leukocyte adhesion deficiency

Periventricular leukomalacia

Neuroacanthocytosis

Leaky gut syndrome

Lhermitte–Duclos disease

Lichen myxedematosus

Lichen sclerosus

Lichen spinulosus

Liddle's syndrome

Li–Fraumeni syndrome

Light chain deposition disease

Limb-girdle muscular dystrophy

Urbach–Wiethe disease

Livedoid dermatitis

Locked-in syndrome

Loa loa filariasis

Loin pain hematuria syndrome

Long QT syndrome

Loose anagen syndrome

Oculocerebrorenal syndrome

Lowry–MacLean syndrome

Levo-Transposition of the great arteries

Lucey–Driscoll syndrome

Problem gambling

Lujan–Fryns syndrome

Lumbar spinal stenosis

Lupus anticoagulant

Toxic epidermal necrolysis

Lymphangiectasia

Lymphangioleiomyomatosis

Lymphatic filariasis

Lymphedema–distichiasis syndrome

Milroy's disease

Congenital lymphedema

Lymphoblastic lymphoma

Lymphocytic colitis

Cutaneous lymphoid hyperplasia

AIDS-related lymphoma

Small cleaved cells

Lymphomatoid papulosis

Lyngstadaas syndrome

Lysosomal storage disease

Macroglobulinemia

Beckwith–Wiedemann syndrome

Macrophagic myofasciitis

May–Hegglin anomaly

Macular corneal dystrophy

Vitelliform macular dystrophy

Bovine spongiform encephalopathy

Benign symmetric lipomatosis

Maffucci syndrome

Mal de debarquement

Pleomorphic undifferentiated sarcoma

Mallory–Weiss syndrome

Malonyl-CoA decarboxylase deficiency

Malouf syndrome

Malpuech facial clefting syndrome

Mandibuloacral dysplasia

Mantle cell lymphoma

Marburg virus disease

Marchiafava–Bignami disease

Marcus Gunn phenomenon

Marden–Walker syndrome

Marek's disease

Marfan syndrome

Loeys–Dietz syndrome

Marinesco–Sjögren syndrome

Maroteaux–Lamy syndrome

Marshall–Smith syndrome

Mass psychogenic illness

Hypermethioninemia

Diabetes mellitus and deafness

Maturity onset diabetes of the young

Binder's syndrome

Müllerian agenesis

McGillivray syndrome

McKusick–Kaufman syndrome

Meadow's syndrome

Medullary cystic kidney disease

Medullary thyroid cancer

Medulloblastoma

Otospondylomegaepiphyseal dysplasia

Megaloblastic anemia

Meige's syndrome

Melkersson–Rosenthal syndrome

Melnick–Needles syndrome

Ménétrier's disease

Ménière's disease

Meningococcal disease

Intellectual disability

Mercury poisoning

Ardalan–Shoja–Kiuru syndrome

Mesenteric ischemia

Metabolic acidosis

Metabolic syndrome

Metachondromatosis

Methylmalonic acidemia

Methylmalonyl-CoA mutase deficiency

Mevalonate kinase deficiency

Relapsing polychondritis

Michelin tire baby syndrome

Michels syndrome

Mickleson syndrome

Microcephaly lymphoedema chorioretinal dysplasia

Macular hypoplasia

Microscopic polyangiitis

Microsporidiosis

Sjögren's syndrome

Microphthalmia–dermal aplasia–sclerocornea syndrome

Benign lymphoepithelial lesion

Mild cognitive impairment

Miller–Dieker syndrome

Minamata disease

Mirhosseini–Holmes–Walton syndrome

Mitochondrial disease

Mitochondrial trifunctional protein deficiency

Mitral valve prolapse

Mixed connective tissue disease

Mixed Müllerian tumor

Mixed receptive-expressive language disorder

Orofaciodigital syndrome 1

Mohr–Tranebjærg syndrome

Molluscum contagiosum

Molybdenum cofactor deficiency

Mondini dysplasia

Mondor's disease

Brunner syndrome

Monoclonal gammopathy of undetermined significance

Motor neuron disease

Tracheobronchomegaly

Moyamoya disease

Myeloperoxidase deficiency

Sanfilippo syndrome

Pityriasis lichenoides et varioliformis acuta

Muckle–Wells syndrome

Hereditary mucoepithelial dysplasia

Pseudo-Hurler polydystrophy

Mucolipidosis type IV

Mucopolysaccharidosis

Multiple sulfatase deficiency

Muenke syndrome

Mulibrey nanism

Multicentric reticulohistiocytosis

Multifocal motor neuropathy

Premature ventricular contraction

Multiple chemical sensitivity

Multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 2

Multiple myeloma

Multiple organ dysfunction syndrome

Multiple sclerosis

Multiple system atrophy

Münchausen syndrome

Münchausen syndrome by proxy

Myasthenia gravis

Mycobacterium avium-intracellulare infection

Atypical pneumonia

Mycosis fungoides

Myelodysplastic syndrome

Myoclonic dystonia

Myoclonic epilepsy

Unverricht–Lundborg disease

Myopathy, X-linked, with excessive autophagy

Myositis ossificans

Inclusion body myositis

Myxoid liposarcoma

N-Acetylglutamate synthase deficiency

Naegeli–Franceschetti–Jadassohn syndrome

Nail–patella syndrome

Nakajo syndrome

Nance–Horan syndrome

Narcissistic personality disorder

Nasodigitoacoustic syndrome

Nasopharynx cancer

Neisseria meningitidis

Nelson's syndrome

Nemaline myopathy

Neonatal diabetes mellitus

Permanent neonatal diabetes mellitus

Transient neonatal diabetes mellitus

Neonatal hemochromatosis

Neonatal hepatitis

Neonatal jaundice

Large for gestational age

Nephrocalcinosis

Nephronophthisis

Hypertensive nephropathy

Nephrotic syndrome

Nerve sheath tumor

Nesidioblastosis

Neural tube defect

Galactosialidosis

Infantile neuroaxonal dystrophy

Neurocutaneous melanosis

Neurofibrillary tangle

Neurofibromatosis

Neurofibromatosis type 3

Neurofibromatosis type 4

Watson syndrome

Malignant peripheral nerve sheath tumor

Neuroleptic malignant syndrome

Nevoid basal cell carcinoma syndrome

Nezelof syndrome

Nicolaides–Baraitser syndrome

Nicotine withdrawal

Niemann–Pick disease

Niemann–Pick disease, type C

X-linked congenital stationary night blindness

Olney's lesions

Noise-induced hearing loss

Non-24-hour sleep–wake disorder

Non-Hodgkin lymphoma

Glycine encephalopathy

Non-small-cell lung carcinoma

Nonverbal learning disorder

Noonan syndrome

Norman–Roberts syndrome

Northern epilepsy syndrome

Notalgia paresthetica

Tree nut allergy

Zonular cataract and nystagmus

Obsessive–compulsive disorder

Obsessive–compulsive personality disorder

Obstructive sleep apnea

Occipital horn syndrome

Occupational asthma

Urofacial syndrome

Pogosta disease

Ocular albinism

Presumed ocular histoplasmosis syndrome

Toxoplasmic chorioretinitis

Oculodentodigital dysplasia

Oculocutaneous albinism type I

Oculomotor nerve palsy

Oculopharyngeal muscular dystrophy

Ogilvie syndrome

Oliver–McFarlane syndrome

Olivopontocerebellar atrophy

Palmoplantar keratoderma

Omsk hemorrhagic fever

Onychogryphosis

Onychomatricoma

Opioid dependence

Opioid-induced hyperalgesia

Opportunistic infection

Oppositional defiant disorder

Opsismodysplasia

Optic disc drusen

Optic nerve hypoplasia

Sugarman syndrome

Oral submucous fibrosis

Organic brain syndrome

Organophosphate poisoning

Ornithine aminotransferase deficiency

Orotic aciduria

Orthostatic intolerance

Osgood–Schlatter disease

Paget's disease of bone

Osteochondritis dissecans

Osteochondritis

Avascular necrosis

Osteopoikilosis

Otodental syndrome

Overwhelming post-splenectomy infection

Primary hypertrophic osteoathropathy

Extramammary Paget's disease

Paget's disease of the breast

Palindromic rheumatism

Pallister–Killian syndrome

Pancreas divisum

Pancreatic cancer

Pancreatoblastoma

Papillon–Lefèvre syndrome

Papular mucinosis

Paracoccidioidomycosis

Paramyotonia congenita

Paraneoplastic cerebellar degeneration

Paranoid personality disorder

List of phobias

Parastremmatic dwarfism

Parathyroid carcinoma

Parathyroid neoplasm

Paratyphoid fever

Parkes Weber syndrome

Parkinson's disease

Paroxysmal cold hemoglobinuria

Paroxysmal nocturnal hemoglobinuria

Ventricular fibrillation

Parry–Romberg syndrome

Intermediate uveitis

Parsonage–Turner syndrome

Passive-aggressive behavior

Patent ductus arteriosus

Patterson syndrome

T-cell acute lymphoblastic leukemia

Pelizaeus–Merzbacher disease

Pelvic inflammatory disease

Pelvic lipomatosis

Pemphigus foliaceus

Pemphigus vulgaris

Pendred syndrome

Penile agenesis and testicular agenesis

Pentalogy of Cantrell

Sensory processing disorder

Polyarteritis nodosa

Labyrinthine fistula

Periodic fever, aphthous stomatitis, pharyngitis and adenitis

Periodic limb movement disorder

Periodontal pathology

Peripartum cardiomyopathy

Peripheral T-cell lymphoma

Pernicious anemia

Peroxisomal disorder

Persistent genital arousal disorder

Persistent truncus arteriosus

Anterior segment mesenchymal dysgenesis

Peutz–Jeghers syndrome

Peyronie's disease

Pfeiffer syndrome

PHACES Syndrome

Phakomatosis pigmentokeratotica

Phakomatosis pigmentovascularis

Medication phobia

Phenylketonuria

Pheochromocytoma

Phosphoglucomutase

Phosphoglycerate kinase

Photosensitive epilepsy

Physical urticaria

Phytophotodermatitis

Pica (disorder)

Pickardt syndrome

Pierre Robin syndrome

Retinitis pigmentosa

Pigment dispersion syndrome

Pigmented villonodular synovitis

Uncombable hair syndrome

Pili multigemini

Pilotto syndrome

Pinta (disease)

Pitt–Hopkins syndrome

Wolf–Hirschhorn syndrome

Pityriasis lichenoides chronica

Pityriasis rubra pilaris

Placental disease

Placental abruption

Plague (disease)

Pneumonic plague

Septicemic plague

Pleural effusion

Gastrointestinal stromal tumor

Plummer–Vinson syndrome

Pneumocystis pneumonia

Pneumonoultramicroscopicsilicovolcanoconiosis

Kindler syndrome

Rothmund–Thomson syndrome

Poland syndrome

Autosomal dominant polycystic kidney

Autosomal recessive polycystic kidney

Polycystic kidney disease

Polycystic ovary syndrome

Polycythemia vera

Polymorphous low-grade adenocarcinoma

Polymyalgia rheumatica

Popliteal pterygium syndrome

Porphyria cutanea tarda

Portal hypertension

Portal vein thrombosis

Rheumatoid factor

Post-polio syndrome

Posttraumatic stress disorder

Tibialis posterior muscle

Posterior urethral valve

Postpartum depression

Selective serotonin reuptake inhibitor

Post-traumatic epilepsy

Orthostatic hypotension

Potassium-aggravated myotonia

Precocious puberty

Progeroid syndromes

Premature ovarian failure

Premenstrual dysphoric disorder

Hypogammaglobulinemia

Primary aldosteronism

Primary cutaneous amyloidosis

Myeloid sarcoma

Primary hyperparathyroidism

Primary lateral sclerosis

Primary progressive aphasia

Pulmonary hypertension

Proximal renal tubular acidosis

Primrose syndrome

Primordial dwarfism

Prinzmetal's angina

Procrastination

Chronic progressive external ophthalmoplegia

Progressive multifocal leukoencephalopathy

Progressive osseous heteroplasia

Progressive muscular atrophy

Progressive supranuclear palsy

Progressive systemic sclerosis

Proliferating trichilemmal cyst

Prolidase deficiency

Prolymphocytic leukemia

Properdin deficiency

Prostate cancer

Protein C deficiency

Protein–energy malnutrition

Protein S deficiency

Prune belly syndrome

Prurigo nodularis

Pseudoachondroplasia

Pseudocholinesterase deficiency

Pseudohermaphroditism

Pseudohypoaldosteronism

Pseudohypoparathyroidism

Pseudomonas infection

Pseudomonas aeruginosa

Pseudomonas stutzeri

Pseudomyxoma peritonei

Pseudopelade of Brocq

Idiopathic intracranial hypertension

Pseudovaginal perineoscrotal hypospadias

Pseudoxanthoma elasticum

Primary polydipsia

Psychosomatic medicine

Puerperal fever

Pulmonary alveolar proteinosis

Pleuropulmonary blastoma

High-altitude pulmonary edema

Pulmonary sequestration

Pulmonary valve stenosis

Pulmonic stenosis

Pure red cell aplasia

Purine nucleoside phosphorylase deficiency

Thrombotic thrombocytopenic purpura

X-linked lymphoproliferative disease

Pycnodysostosis

Pyoderma gangrenosum

Hereditary pyropoikilocytosis

Pyruvate carboxylase deficiency

Pyruvate dehydrogenase deficiency

Pyruvate kinase deficiency

Retrieved from "https://en.wikipedia.org/w/index.php?title=User:Drsalmanshah165/Books/Medical_Wikipedia_0-P&oldid=836134533"

User namespace book pages