Terminology Service for NFDI4Health
Mental Retardation, X-linked 102
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http://purl.obolibrary.org/obo/NCIT_C129931
An inherited condition caused by mutation(s) in the DDX3X gene, encoding ATP-dependent RNA helicase DDX3X. It is characterized by severe intellectual disability and variable neurologic features. [ ]
Term info
Label
Mental Retardation, X-linked 102
Synonyms
- Mental Retardation, X-linked 102
NCI META CUI
CL513033
Preferred Name
Mental Retardation, X-linked 102
Semantic Type
Disease or Syndrome
code
C129931