Dermoodontodysplasia

Preferred Label : Dermoodontodysplasia;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Ectodermal dysplasia, hair-nail-tooth type;

Inheritance : Autosomal dominant;

Prefixed ID : %125640;

Details

Origin ID

125640;

UMLS CUI

C1852144;

Automatic exact mappings (from CISMeF team)
- Dermodental dysplasia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Dermo-odonto dysplasia (disorder) [SNOMED CT concept]
- Dermo-odontodysplasia [ICD-11 More detail]
- Dermoodontodysplasia [ORDO Disease]
- dermoodontodysplasia [MeSH concept]
- dermoodontodysplasia [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dry skin [HPO term]
- Ectodermal dysplasia [HPO term]
- Hypodontia [HPO term]
- Mild variable ectodermal dysplasia [HPO term]
- Nail dysplasia [HPO term]
- Thin skin [HPO term]
- Trichodysplasia [HPO term]
ORDO concept(s)
- Dermoodontodysplasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dermo-odonto dysplasia (disorder) [SNOMED CT concept]
- Dermoodontodysplasia [ORDO Disease]
- dermoodontodysplasia [MeSH Supplementary Concept]
- dermoodontodysplasia [MeSH concept]

Keyword's position in hierarchy(ies) :

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