All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04105 CJS;PHS-2 Culler-Jones syndrome (CJS, Pallister-Hall syndrome type 2 (PHS-2)) 615849 - 0 0 GLI2 - -
00438 HPE holoprosencephaly (HPE) 236100 - 7 7 GLI2, SHH, SIX3, TGIF1, ZIC2 - -
02986 HPE-9 holoprosencephaly, type 9 (HPE-9) 610829 - 0 0 GLI2 - -
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