Camptobrachydactyly

Preferred Label : Camptobrachydactyly;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %114150;

Details

Origin ID

114150;

UMLS CUI

C1861963;

Currated CISMeF NLP mapping
- Camptobrachydactyly [MeSH concept]
- Camptobrachydactyly [ORDO Disease]
- Camptobrachydactyly (disorder) [SNOMED CT concept]
- camptobrachydactyly [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Brachydactyly [HPO term]
- Brachydactyly of hands and feet [HPO term]
- Congenital finger flexion contractures [HPO term]
- Hand polydactyly [HPO term]
- Septate vagina [HPO term]
- Short toe [HPO term]
- Syndactyly [HPO term]
- Urinary incontinence [HPO term]
ORDO concept(s)
- Camptobrachydactyly [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Camptobrachydactyly [ORDO Disease]
- Camptobrachydactyly [MeSH concept]
- Camptobrachydactyly (disorder) [SNOMED CT concept]
- camptobrachydactyly [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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