Terminology Service for NFDI4Health
Mental Retardation, Autosomal Dominant 39
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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. [ ]
Term info
Label
Mental Retardation, Autosomal Dominant 39
Synonyms
- MRD39
- Mental Retardation, Autosomal Dominant 39
Preferred Name
Mental Retardation, Autosomal Dominant 39
Semantic Type
Disease or Syndrome
UMLS CUI
C4225296
code
C156309