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Schilbach-Rott syndrome
Disease Summary
Associated Targets ()
Mondo Description Schilbach-Rott syndrome (SRS) is an autosomal dominant dysmorphic disorder that is characterized by dysmorphic facies with hypotelorism, blepharophimosis, and cleft palate, and the frequent occurrence of hypospadias in males.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0002930
MESH:C563509
OMIM:164220
Orphanet:2353
SCTID:721902002
MONDO:0008113
High level summary of knowledge for a disease, including descriptions and datasource references.