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
01045 GBBB2 Opitz GBBB syndrome, type 2, autosomal dominant (GBBB2) 145410 AD 2 2 HIRA, SPECC1L - -
02296 OBLFC1 facial clefting, oblique, type 1 (OBLFC1, oculomaxillofacial dysplasia) 600251 AD 3 3 SPECC1L - -
05915 TBHS hypertelorism, Teebi type syndrome (TBHS) - AD 1 1 SPECC1L - -
06534 TBHS Hypertelorism, Teebi type 145420 AD - - SPECC1L - -
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