All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01399 - Single upper central incisor 147250 - - - SHH - -
02064 - Schizencephaly 269160 - - - EMX2, SHH, SIX3 - -
00438 HPE holoprosencephaly (HPE) 236100 - - - GLI2, SHH, SIX3, TGIF1, ZIC2 - -
01368 HPE-3 holoprosencephaly, type 3 (HPE-3) 142945 - - - SHH - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
03045 MCOPCB-5 microphthalmia, isolated, with coloboma, type 5 (MCOPCB-5) 611638 - - - SHH - -
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