Alopecia areata 2

Preferred Label : Alopecia areata 2;

Symbol : AA2;

CISMeF acronym : AA2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of alopecia areata, see 104000.;

Inheritance : Autosomal recessive; Autosomal dominant;

Prefixed ID : %610753;

Details

Origin ID

610753;

UMLS CUI

C1853104;

Automatic exact mappings (from CISMeF team)
- AA1-3 protocol [MeSH Supplementary Concept]
- Alopecia totalis [ORDO Disease]
- Neurofibromatosis type 2 (disorder) [SNOMED CT concept]
- pharyngeal arch artery 2 [UBERON concept]
Currated CISMeF NLP mapping
- alopecia areata 2 [MeSH concept]
- alopecia areata 2 [MeSH Supplementary Concept]
DO Cross reference
- alopecia areata [DO Concept]
HPO term(s)
- Alopecia of scalp [HPO term]
- Alopecia totalis [HPO term]
- Alopecia universalis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Autosomal recessive inheritance [HPO term]
- Incomplete penetrance [HPO term]
- Multifactorial inheritance [HPO term]
- Patchy alopecia [HPO term]
ORDO concept(s)
- Alopecia totalis [ORDO Disease]
- Alopecia universalis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- alopecia areata 2 [MeSH Supplementary Concept]
- alopecia areata 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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