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X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiovascular septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding.
Mondo Term and Equivalent IDs
MONDO:0018569:  X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome
Orphanet:435938: 
UMLS:CN237580: