Intellectual developmental disorder, autosomal dominant 67

Preferred Label : Intellectual developmental disorder, autosomal dominant 67;

Symbol : MRD67;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Mental retardation, autosomal dominant 67;

Prefixed ID : #619927;

Details

Origin ID

619927;

UMLS CUI

C5677006;

Genes related to phenotype
- Glutamate receptor, ionotropic, ampa 1 [OMIM gene]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]

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