Aredyld - CISMeF

Preferred Label : Aredyld;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes;

Inheritance : Autosomal recessive;

Prefixed ID : 207780;

Détails

Origin ID

207780;

UMLS CUI

C0342280;

Currated CISMeF NLP mapping
- AREDYLD Syndrome [MeSH concept]
- AREDYLD syndrome [ICD-11 More detail]
- AREDYLD syndrome [MeSH Supplementary Concept]
- AREDYLD syndrome [ORDO Disease]
- Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes (disorder) [SNOMED CT concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Abnormality of the ear [HPO term]
- Autosomal recessive inheritance [HPO term]
- Ectodermal dysplasia [HPO term]
- Generalized hypotrichosis [HPO term]
- Mandibular prognathia [HPO term]
ORDO concept(s)
- AREDYLD syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- AREDYLD Syndrome [MeSH concept]
- AREDYLD syndrome [ORDO Disease]
- AREDYLD syndrome [MeSH Supplementary Concept]
- Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes (disorder) [SNOMED CT concept]

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

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