All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06870 HPE13 Holoprosencephaly 13, X-linked 301043 - 1 1 STAG2 - -
06862 MKMS Mullegama-Klein-Martinez syndrome 301022 XL - - STAG2 - -
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