Psoriasis 2 - CISMeF

Preferred Label : Psoriasis 2;

Symbol : PSORS2;

CISMeF acronym : PSORS2;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the caspase recruitment domain-containing protein-14 gene (CARD14, 607211.0001);

Prefixed ID : #602723;

Details

Origin ID

602723;

UMLS CUI

C1864497;

Automatic exact mappings (from CISMeF team)
- CARD14 wt Allele [NCIt concept]
- psoriasis 2 [DO Concept]
- symbol withdrawn PSORS2 [HGNC gene]
Broader ORDO disease(s)
- Adult psoriatic arthritis [ORDO Disease]
DO Cross reference
- psoriasis 2 [DO Concept]
Genes related to phenotype
- Caspase recruitment domain-containing protein 14 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Epidermal acanthosis [HPO term]
- Hyperkeratosis [HPO term]
- Parakeratosis [HPO term]
- Psoriasiform dermatitis [HPO term]
- Scaling skin [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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