Hypotrichosis - CISMeF

Preferred Label : Hypotrichosis;

NCIt definition : A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body.;

Détails

Origin ID

C34720;

UMLS CUI

C4721530;

Currated CISMeF NLP mapping
- HYPOTRICHOSIS [WHO-ART High Level Term]
- Hypotrichosis [PASCAL descriptor]
- Hypotrichosis [HPO term]
- Hypotrichosis [MedDRA Preferred Term]
- Hypotrichosis (disorder) [SNOMED CT concept]
- hypotrichosis [DO Concept]
- hypotrichosis [Disease (Nov.)]
- hypotrichosis [MeSH Descriptor]
- hypotrichosis [MeSH concept]
- hypotrichosis, nos [SNOMED Notion]
Has associated anatomic sites
- Integumentary System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital hypotrichia (disorder) [SNOMED CT concept]
- HYPOTRICHOSIS [WHO-ART High Level Term]
- Hypotrichosis [HPO term]
- Hypotrichosis [PASCAL descriptor]
- Hypotrichosis [MedDRA Preferred Term]
- Hypotrichosis (disorder) [SNOMED CT concept]
- congenital hypotrichia [SNOMED Notion]
- hypotrichosis [DO Concept]
- hypotrichosis [Disease (Nov.)]
- hypotrichosis [MeSH Descriptor]
- hypotrichosis [MeSH concept]
- hypotrichosis, nos [SNOMED Notion]
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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