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Up to: Congenital nervous system disorder · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Autosomal dominant syndromic intellectual disability · Houge-Janssens syndrome
Houge-Janssens syndrome 1
An autosomal dominant intellectual developmental disorder that has material basis in an autosomal dominant mutation of the PPP2R5D gene on chromosome 6p21.1.
This condition has no sub-types.