Dysplasia epiphysealis hemimelica

Preferred Label : Dysplasia epiphysealis hemimelica;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Trevor disease;

Inheritance : No familial case reported;

Prefixed ID : 127800;

Détails

Origin ID

127800;

UMLS CUI

C0432282;

Automatic exact mappings (from CISMeF team)
- Dysplasia epiphysealis hemimelica [ACR pathology]
Currated CISMeF NLP mapping
- Dysplasia epiphysealis hemimelica [ICD-11 More detail]
- Dysplasia epiphysealis hemimelica [MeSH concept]
- Dysplasia epiphysealis hemimelica [ORDO Disease]
- Dysplasia epiphysealis hemimelica (disorder) [SNOMED CT concept]
- Dysplasia epiphysialis hemimelica [PASCAL descriptor]
- dysplasia epiphysealis hemimelica [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Overgrowth [HPO term]
ORDO concept(s)
- Dysplasia epiphysealis hemimelica [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dysplasia epiphysealis hemimelica [ORDO Disease]
- Dysplasia epiphysealis hemimelica [MeSH concept]
- Dysplasia epiphysealis hemimelica (disorder) [SNOMED CT concept]
- dysplasia epiphysealis hemimelica [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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