Pachydermodactyly, familial

Preferred Label : Pachydermodactyly, familial;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? Autosomal dominant;

Prefixed ID : 600356;

Details

Origin ID

600356;

UMLS CUI

C1838218;

Currated CISMeF NLP mapping
- pachydermodactyly, familial [MeSH concept]
- pachydermodactyly, familial [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- pachydermodactyly, familial [MeSH Supplementary Concept]
- pachydermodactyly, familial [MeSH concept]

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