Congenital Alopecia

Preferred Label : Congenital Alopecia;

NCIt definition : A congenital condition characterized by the absence of hair on the scalp or entire body. The lack of hair is rarely absolute and is usually accompanied by incompletely grown, lanugo-like hair. It affects males twice as much as females and a familial tendency is common.;

Détails

Origin ID

C35790;

UMLS CUI

C0265992;

Automatic exact mappings (from CISMeF team)
- Congenital alopecia [MedDRA Preferred Term]
- congenital alopecia X-linked [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Alopecia, congenital [OMIM Phenotype]
- Atrichia congenita (disorder) [SNOMED CT concept]
- Congenital alopecia [ICD-10 Sub-category]
- Congenital alopecia [ICD-10 Sub-category (who)]
- Congenital alopecia (disorder) [SNOMED CT concept]
- congenital alopecia [SNOMED Notion]
Has associated anatomic sites
- Integumentary System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Alopecia, congenital [OMIM Phenotype]
- Atrichia congenita (disorder) [SNOMED CT concept]
- Congenital alopecia [ICD-10 Sub-category]
- Congenital alopecia [ICD-10 Sub-category (who)]
- Congenital alopecia (disorder) [SNOMED CT concept]
- congenital alopecia [SNOMED Notion]
Validated automatic mappings to BTNT
- Congenital alopecia X-linked [MeSH concept]
- congenital alopecia X-linked [MeSH Supplementary Concept]
disease_has_finding
- Cutaneous Involvement [NCIt concept]
disease_has_primary_anatomic_site
- Hair [NCIt concept]
- Skin [NCIt concept]

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

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