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Mental Retardation, Autosomal Dominant 39

^ http://purl.obolibrary.org/obo/NCIT_C156309


An autosomal dominant condition caused by mutation(s) in the MYT1L gene, encoding myelin transcription factor 1-like protein. It is characterized by intellectual disability and mild dysmorphic facial features. [ NCI ]

Synonyms: Mental Retardation, Autosomal Dominant 39, MRD39

Term info

Preferred Name

Mental Retardation, Autosomal Dominant 39

Semantic Type

Disease or Syndrome

UMLS CUI

C4225296

code

C156309