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
02064 - Schizencephaly 269160 - 0 0 EMX2, SHH, SIX3 - -
00438 HPE holoprosencephaly (HPE) 236100 - 14 13 GLI2, SHH, SIX3, TGIF1, ZIC2 - -
01368 HPE3 holoprosencephaly, type 3 (HPE-3) 142945 AD 1 0 SHH - -
00139 ID intellectual disability (ID) - - 2195 1894 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 540 more - -
03045 MCOPCB5 microphthalmia, isolated, with coloboma, type 5 (MCOPCB-5) 611638 AD 1 0 SHH - -
01399 SMMCI single median maxillary central incisor 147250 AD 0 0 SHH - -
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