Keratosis palmoplantaris striata III

Preferred Label : Keratosis palmoplantaris striata III;

Symbol : PPKS3;

CISMeF acronym : KPPS3; PPKS3; SPPK3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Keratoderma, palmoplantar, striate form III; KPPS3; SPPK3; Striate palmoplantar keratoderma III;

Prefixed ID : #607654;

Details

Origin ID

607654;

UMLS CUI

C2931123;

Automatic exact mappings (from CISMeF team)
- Striate palmoplantar keratoderma [PASCAL descriptor]
- keratosis palmoplantaris striata 3 [MeSH Supplementary Concept]
Broader ORDO disease(s)
- Striate palmoplantar keratoderma [ORDO Disease]
Genes related to phenotype
- Keratin 1, type II [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Palmoplantar keratoderma [HPO term]
Not associated HPO term(s)
- Abnormal hair morphology [HPO term]
- Abnormality of the nail [HPO term]
ORDO concept(s)
- Striate palmoplantar keratoderma [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Keratosis palmoplantaris striata 3 [MeSH concept]
- keratosis palmoplantaris striata 3 [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients