Lelis syndrome

Preferred Label : Lelis syndrome;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Ectodermal dysplasia, hypohidrotic, with acanthosis nigricans;

Prefixed ID : %608290;

Détails

Origin ID

608290;

UMLS CUI

C1842307;

Currated CISMeF NLP mapping
- Ectodermal dysplasia - acanthosis nigricans [ICD-11 More detail]
- Ectodermal dysplasia with acanthosis nigricans syndrome (disorder) [SNOMED CT concept]
- Lelis syndrome [ORDO Disease]
- lelis syndrome [MeSH concept]
- lelis syndrome [MeSH Supplementary Concept]
ORDO concept(s)
- Lelis syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ectodermal dysplasia - acanthosis nigricans [ICD-11 More detail]
- Ectodermal dysplasia with acanthosis nigricans syndrome (disorder) [SNOMED CT concept]
- Lelis syndrome [ORDO Disease]
- lelis syndrome [MeSH Supplementary Concept]
- lelis syndrome [MeSH concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients