All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02064 - Schizencephaly 269160 - 0 0 EMX2, SHH, SIX3 - -
00438 HPE holoprosencephaly (HPE) 236100 - 14 13 GLI2, SHH, SIX3, TGIF1, ZIC2 - -
01439 HPE2 holoprosencephaly, type 2 (HPE-2) 157170 AD 0 0 SIX3 - -
00139 ID intellectual disability (ID) - - 2334 2032 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 542 more - -
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