All diseases

10 entries on 1 page. Showing entries 1 - 10.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03411 ACNINV3 acne inversa, familial, type 3 (ACNINV-3) 613737 AD - - PSEN1 - -
00095 AD3 Alzheimer disease, type 3 (protection against, due to APOE3-Christchurch) 607822 AD 34 515 APOE, PSEN1 - -
03394 CMD1U cardiomyopathy, dilated, type 1U CMD-1U) 613694 AD - - PSEN1 - -
00115 CRMCC microangiopathy, cerebroretinal, with calcifications and cysts (CRMCC, Coats plus syndrome) 612199 AR 33 32 CTC1, OBFC1, TEN1 - -
06539 ECTD13 Ectodermal dysplasia 13, hair/tooth type 617392 AR 2 2 KREMEN1 - -
05108 ECTDO dysplasia, ectodermal, with oligodontia (ECTDO) - - 4 4 KREMEN1 - -
00096 FTD dementia, frontotemporal (FTD) 600274 AD 429 61 MAPT, PSEN1 - -
00426 MEN1 neoplasia, endocrine, multiple, type 1 (MEN-1, Wermer syndrome) 131100 AD 542 549 MEN1 - autosomal dominant
06011 PCH2F hypoplasia, pontocerebellar, type 2F 617026 AR - - TSEN15 - -
01505 Picks Pick disease 172700 AD 5 1 MAPT, PSEN1 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.