| | Disease name | Disease category |
Salmonella | H00113 | Salmonellosis | Bacterial infectious disease |
HIV | H01563 | HIV infection | Viral infectious disease |
Escherichia | H00277 | Enterohemorrhagic Escherichia coli (EHEC) infection | Bacterial infectious disease |
| H00278 | Enteropathogenic Escherichia coli (EPEC) infection | Bacterial infectious disease |
HTLV-1 | H00009 | Adult T-cell leukemia | Cancer |
IMD57 | H02525 | Disorders of innate immunity | Immune system disease |
TRAPS/MS5 | H00912 | Tumor necrosis factor receptor-associated periodic syndrome | Immune system disease |
| H01490 | Multiple sclerosis | Immune system disease |
EDAID1/IP | H00540 | Osteoporosis, lymphedema, anhydrotic ectodermal dysplasia with immunodeficiency (OLEDAID) | Congenital malformation |
| H00645 | Incontinentia pigmenti | Congenital malformation |
EDAID1 | H00540 | Osteoporosis, lymphedema, anhydrotic ectodermal dysplasia with immunodeficiency (OLEDAID) | Congenital malformation |
CMCU | H02593 | Chronic mucocutaneous ulceration | Immune system disease |
KSHV | H00041 | Kaposi sarcoma | Cancer |
EBV | H00008 | Burkitt lymphoma | Cancer |
| H00007 | Hodgkin lymphoma | Cancer |
| H00054 | Nasopharyngeal cancer | Cancer |
HCV | H00048 | Hepatocellular carcinoma | Cancer |
Shigella | H00299 | Shigellosis | Bacterial infectious disease |
Escherichia/Shigella | H00277 | Enterohemorrhagic Escherichia coli (EHEC) infection | Bacterial infectious disease |
| H00278 | Enteropathogenic Escherichia coli (EPEC) infection | Bacterial infectious disease |
| H00299 | Shigellosis | Bacterial infectious disease |
HCMV | H00368 | Cytomegalovirus infection | Viral infectious disease |
PGBM1 | H01744 | Polyglucosan body myopathy | Immune system disease |
AIPDS | H02414 | Autoinflammation, panniculitis, and dermatosis syndrome | Immune system disease |
AIFBL1 | H02592 | Familial Behcet-like autoinflammatory syndrome | Immune system disease |
AIEFL | H02620 | Autoinflammation with episodic fever and lymphadenopathy | Immune system disease |
XLP2 | H01969 | X-linked lymphoproliferative syndrome | Primary immunodeficiency |
ECTD1/STHAGX1 | H00651 | Hypohidrotic ectodermal dysplasia | Congenital malformation |
| H00625 | Tooth agenesis | Congenital malformation |
ECTD10 | H00651 | Hypohidrotic ectodermal dysplasia | Congenital malformation |
ECTD11 | H00651 | Hypohidrotic ectodermal dysplasia | Congenital malformation |
HIGM1 | H00086 | Immunodeficiency with hyper-IgM | Immune system disease |
HIGM3 | H00086 | Immunodeficiency with hyper-IgM | Immune system disease |
OPTB2 | H00436 | Osteopetrosis | Congenital malformation |
OPTB7 | H00436 | Osteopetrosis | Congenital malformation |
PDB2/FEO | H00437 | Paget disease of bone | Musculoskeletal disease |
| H02042 | Familial expansile osteolysis | Musculoskeletal disease |
IMD16 | H00093 | Combined immunodeficiency | Primary immunodeficiency |
LPFS3 | H01970 | Lymphoproliferative syndrome | Primary immunodeficiency |
LPFS2 | H01970 | Lymphoproliferative syndrome | Primary immunodeficiency |
CVID2 | H00088 | Common variable immunodeficiency | Immune system disease |
CVID4 | H00088 | Common variable immunodeficiency | Immune system disease |
HPV | H00030 | Cervical cancer | Cancer |
HSV | H00365 | Herpes simplex virus infection | Viral infectious disease |