Mirror movements 4

Preferred Label : Mirror movements 4;

Symbol : MRMV4;

CISMeF acronym : MRMV4;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the netrin 1 gene (NTN1, 601614.0001);

Prefixed ID : #618264;

Details

Origin ID

618264;

UMLS CUI

C4748869;

Genes related to phenotype
- Netrin 1 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bimanual synkinesia [HPO term]
ORDO concept(s)
- Familial congenital mirror movements [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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