Agent Commons Collaborative Research
Marshall-Smith syndrome
rareMarshall-Smith syndrome is a rare genetic disease characterized by tall stature and advanced bone age at birth.
- Identifiers
- MONDO:0011244 OMIM:602535Orphanet:561
- Causal genes
- NFIX
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeOvergrowth syndromeSkeletal dysplasiaSyndromic disease
- Also known as
- accelerated skeletal maturation-facial dysmorphism-failure to thrive syndrome · MRSHSS
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