Scalp defects and postaxial polydactyly

Preferred Label : Scalp defects and postaxial polydactyly;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 181250;

Details

Origin ID

181250;

UMLS CUI

C1867021;

HPO term(s)
- Aplasia cutis congenita of scalp [HPO term]
- Autosomal dominant inheritance [HPO term]
- Postaxial polydactyly type A [HPO term]
ORDO concept(s)
- Scalp defects-postaxial polydactyly syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Scalp defects postaxial polydactyly [MeSH concept]
- Scalp defects-postaxial polydactyly syndrome [ORDO Disease]
- scalp defects postaxial polydactyly [MeSH Supplementary Concept]

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