Mononeuropathy of the median nerve, mild

Preferred Label : Mononeuropathy of the median nerve, mild;

Symbol : MNMN;

CISMeF acronym : MNMN;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Carpal tunnel syndrome, susceptibility to;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the SH3 domain and tetratricopeptide repeat domain 2 gene (SH3TC2, 608206.0005);

Prefixed ID : #613353;

Details

Origin ID

613353;

UMLS CUI

C3150596;

Genes related to phenotype
- Sh3 domain and tetratricopeptide repeat domain 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Constrictive median neuropathy [HPO term]
- Mononeuropathy [HPO term]
- Peripheral axonal neuropathy [HPO term]
- Polyneuropathy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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