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
01869 - Hamartoma of hypothalamus 241800 - 0 0 GLI3 - -
00297 GCPS cephalopolysyndactyly, Greig syndrome (GCPS) 175700 - 55 55 GLI3 - -
00139 ID intellectual disability (ID) - - 2099 1812 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 537 more - -
00300 PAPA-1;PAPB polydactyly, postaxial, type A1 (PAPA-1, type B included (PAPB)) 174200 - 1 1 GLI3 - autosomal dominant
00299 PHS Pallister-Hall syndrome (PHS) 146510 - 25 22 GLI3 - -
00301 PPD4 polydactyly, preaxial, type IV (PPD4) 174700 AD 1 1 GLI3 - -
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