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
06135 CUGS Cardiac-urogenital syndrome 618280 AD - - C11orf9 - -
05477 MMERV encephalitis/encephalopathy, mild, with reversible myelin vacuolization (MMERV) 618113 AD - - C11orf9 - autosomal dominant
05478 TAPVR1 pulmonary venous return, total anomalous, type 1 (TAPVR-1, Scimitar syndrome) 106700 - - - C11orf9 - -
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