Polydactyly, postaxial, type a2

Preferred Label : Polydactyly, postaxial, type a2;

Symbol : PAPA2;

CISMeF acronym : PAPA2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Postaxial polydactyly, type a2;

Description : For a phenotypic description and a discussion of genetic heterogeneity of postaxial polydactyly, see 174200.;

Inheritance : Autosomal dominant;

Prefixed ID : %602085;

Details

Origin ID

602085;

UMLS CUI

C1865883;

Currated CISMeF NLP mapping
- polydactyly, postaxial, type A2 [MeSH concept]
- polydactyly, postaxial, type A2 [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Postaxial hand polydactyly [HPO term]
ORDO concept(s)
- Postaxial polydactyly type A [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- polydactyly, postaxial, type A2 [MeSH Supplementary Concept]
- polydactyly, postaxial, type A2 [MeSH concept]
Validated automatic mappings to NTBT
- Postaxial polydactyly type A [ORDO Disease]

Keyword's position in hierarchy(ies) :

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