White sponge nevus 2

Preferred Label : White sponge nevus 2;

Symbol : WSN2;

CISMeF acronym : WSN2;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the keratin-13 gene (KRT13, 148065.0001);

Prefixed ID : #615785;

Details

Origin ID

615785;

UMLS CUI

C4014321;

DO Cross reference
- hereditary mucosal leukokeratosis [DO Concept]
Genes related to phenotype
- Keratin 13, type I [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Edema [HPO term]
- Epidermal acanthosis [HPO term]
- Hyperparakeratosis [HPO term]
ORDO concept(s)
- White sponge nevus [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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