All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02551 BCC1 carcinoma, basal cell, susceptibility to, type 1 (BCC-1) 605462 - 10 10 PTCH1, PTCH2, RASA1, SMO - -
05225 CRJS Curry-Jones syndrome, somatic mosaic (CRJS) 601707 - 8 8 SMO - -
01281 DTDP1 dysplasia, dentin, type I (DTDP1) 125400 AR - - SMOC2 - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
06617 MCCPD Microcephaly, congenital cataract, and psoriasiform dermatitis 616834 AR - - MSMO1 - -
01660 MLA microphthalmia, with limb anomalies (MLA, anophthalmia) 206920 AR - - SMOC1 - -
01869 PHLS Pallister-Hall-like syndrome 241800 AR - - SMO - -
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