All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01045 GBBB2 syndrome, Opitz GBBB, type 2, autosomal dominant (GBBB2) 145410 AD 2 2 HIRA, SPECC1L - -
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