Intellectual developmental disorder, autosomal dominant 68

Preferred Label : Intellectual developmental disorder, autosomal dominant 68;

Symbol : MRD68;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Mental retardation, autosomal dominant 68;

Prefixed ID : #619934;

Details

Origin ID

619934;

UMLS CUI

C5677008;

Genes related to phenotype
- Lysine-specific methyltransferase 2b [OMIM gene]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]

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