Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly

Preferred Label : Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly;

Symbol : MRT75;

Type : Phenotype, molecular basis known;

Prefixed ID : #619827;

Details

Origin ID

619827;

UMLS CUI

C5676961;

Genes related to phenotype
- P53-induced death domain protein 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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