Intellectual developmental disorder, autosomal recessive 76

Preferred Label : Intellectual developmental disorder, autosomal recessive 76;

Symbol : MRT76;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Mental retardation, autosomal recessive 76;

Prefixed ID : #619931;

Details

Origin ID

619931;

UMLS CUI

C5677007;

Genes related to phenotype
- Glutamate receptor, ionotropic, ampa 1 [OMIM gene]
ORDO concept(s)
- Autosomal recessive non-syndromic intellectual disability [ORDO Disease]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]

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