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global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal dominant syndrome characterized by underdevelopment of the corpus callosum, mild to moderate developmental delay and intellectual disability, variable microcephaly or mild macrocephaly, short stature, feeding problems, facial dysmorphisms, and cardiac and renal malformations.
Mondo Term and Equivalent IDs
MONDO:0014994:  global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies
UMLS:C4310644: