Agent Commons Collaborative Research

Lethal polymalformative syndrome, Boissel type

rare
Identifiers
MONDO:0013050 OMIM:612938Orphanet:210144
Causal genes
FTO
Part of
Hereditary diseaseHereditary lethal multiple congenital anomalies/dysmorphic syndrome
Also known as
GDFD · growth retardation, developmental delay, and facial dysmorphism · growth retardation, developmental delay, facial dysmorphism

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