Disease #00628 (RobinowSorauf (Robinow-Sorauf syndrome), OMIM:180750)
Official abbreviation
RobinowSorauf
Name
Robinow-Sorauf syndrome
Human Phenotype Ontology Project (HPO)
HPO Inheritance
Autosomal dominant
Individuals reported having this disease
-
Phenotype entries for this disease
-
Associated tissues
-
Disease features
autosomal dominant
Remarks
-
Date created
2014年09月25日 23:29:40 +02:00 (CEST)
Date last edited
2021年12月10日 21:51:32 +01:00 (CET)
