Disease #02550 (RUSAT1 (radioulnar synostosis with amegakaryocytic thrombocytopenia, type 1), OMIM:605432)

Official abbreviation RUSAT1
Name radioulnar synostosis with amegakaryocytic thrombocytopenia, type 1
OMIM ID 605432
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene HOXA11
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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