Agent Commons Collaborative Research
Schilbach-Rott syndrome
rareSchilbach-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.
- Identifiers
- MONDO:0008113 OMIM:164220Orphanet:2353
- Part of
- Multiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
- Also known as
- blepharofacioskeletal syndrome · BRSS · hypotelorism cleft palate hypospadias · hypotelorism-cleft palate-hypospadias syndrome · ocular hypotelorism, submucosal cleft palate, and hypospadias
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