Ectodermal dysplasia, trichoodontoonychial type

Preferred Label : Ectodermal dysplasia, trichoodontoonychial type;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 129510;

Details

Origin ID

129510;

UMLS CUI

C1851858;

Currated CISMeF NLP mapping
- Ectodermal dysplasia trichoodontoonychial type (disorder) [SNOMED CT concept]
- Ectodermal dysplasia, trichoodontoonychial type [ORDO Disease]
- Tricho-odonto-onychial ectodermal dysplasia [ICD-11 More detail]
- ectodermal dysplasia, trichoodontoonychial type [MeSH concept]
- ectodermal dysplasia, trichoodontoonychial type [MeSH Supplementary Concept]
HPO term(s)
- Abnormal thorax morphology [HPO term]
- Absent nipple [HPO term]
- Autosomal dominant inheritance [HPO term]
- Ectodermal dysplasia [HPO term]
- Hypodontia [HPO term]
- Hypotrichosis [HPO term]
- Irregular hyperpigmentation of back [HPO term]
- Mild neurosensory hearing impairment [HPO term]
- Sparse hair [HPO term]
Not associated HPO term(s)
- Abnormal sweat gland morphology [HPO term]
- Hyperhidrosis [HPO term]
ORDO concept(s)
- Ectodermal dysplasia, trichoodontoonychial type [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ectodermal dysplasia trichoodontoonychial type (disorder) [SNOMED CT concept]
- Ectodermal dysplasia, trichoodontoonychial type [ORDO Disease]
- ectodermal dysplasia, trichoodontoonychial type [MeSH Supplementary Concept]
- ectodermal dysplasia, trichoodontoonychial type [MeSH concept]

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