Alopecia, congenital

Preferred Label : Alopecia, congenital;

Symbol : ALPC;

CISMeF acronym : ALPC;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked;

Prefixed ID : 300042;

Details

Origin ID

300042;

UMLS CUI

C0265992;

Currated CISMeF NLP mapping
- Atrichia congenita (disorder) [SNOMED CT concept]
- Congenital Alopecia [NCIt concept]
- Congenital alopecia [ICD-10 Sub-category]
- Congenital alopecia [ICD-10 Sub-category (who)]
- Congenital alopecia (disorder) [SNOMED CT concept]
- congenital alopecia [SNOMED Notion]
HPO term(s)
- Alopecia [HPO term]
- Hypotrichosis [HPO term]
- Severe hypotrichosis [HPO term]
- Sparse hair [HPO term]
- X-linked inheritance [HPO term]
Not associated HPO term(s)
- Abnormal eyebrow morphology [HPO term]
- Abnormal eyelash morphology [HPO term]
ORDO concept(s)
- Alopecia totalis [ORDO Disease]
See also inter- (CISMeF)
- Alopecia totalis [ORDO Disease]
- Alopecia totalis [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Atrichia congenita (disorder) [SNOMED CT concept]
- Congenital Alopecia [NCIt concept]
- Congenital alopecia [ICD-10 Sub-category (who)]
- Congenital alopecia [ICD-10 Sub-category]
- 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]

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