Palmoplantar keratoderma, punctate type II

Preferred Label : Palmoplantar keratoderma, punctate type II;

Symbol : PPKP2;

CISMeF acronym : PPKP2; PPPP;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : PPPP; Porokeratosis punctata palmaris et plantaris;

Inheritance : Autosomal dominant;

Prefixed ID : %175860;

Details

Origin ID

175860;

UMLS CUI

C1867982;

Automatic exact mappings (from CISMeF team)
- punctate palmoplantar keratoderma type II [DO Concept]
Broader ORDO disease(s)
- Isolated punctate palmoplantar keratoderma [ORDO Disease]
Currated CISMeF NLP mapping
- Punctate palmoplantar keratoderma type 2 [ORDO Disease]
DO Cross reference
- punctate palmoplantar keratoderma type II [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Porokeratosis [HPO term]
- Spinous keratoses of palms and soles [HPO term]
ORDO concept(s)
- Punctate palmoplantar keratoderma type 2 [ORDO Disease]
See also inter- (CISMeF)
- Porokeratosis of Mantoux (disorder) [Inactive SNOMED CT concept]
- Porokeratosis punctata palmaris et plantaris [MeSH concept]
- pneumococcal purpura-producing principle [MeSH concept]
- pneumococcal purpura-producing principle [MeSH Supplementary Concept]
- porokeratosis of Mantoux [Disease (Nov.)]
- porokeratosis punctata palmaris et plantaris [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Porokeratosis punctata palmaris et plantaris [MeSH concept]
- Punctate palmoplantar keratoderma type 2 [ORDO Disease]
- Punctate palmoplantar keratoderma type 2 (disorder) [SNOMED CT concept]
- porokeratosis punctata palmaris et plantaris [MeSH Supplementary Concept]

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