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
04327 CRS craniosynostosis (CRS) - - 64 46 TCF12 - -
00530 CRS3 craniosynostosis, type 3 615314 AD 8 7 TCF12 - variable craniosynostosis individually or in combination, coronal and/or agittal skull sutures; congenital dysmorphisms (brachydactyly, ptosis, strabismus); neurodevelopmental impairment may be present
07148 HH hypogonadotropic hypogonadism - - 1 1 TCF12 - -
07147 HH26 hypogonadotropic hypogonadism, type 26, with or without anosmia 619718 AD;AR - - TCF12 - -
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