Alopecia-intellectual disability syndrome 2

Preferred Label : Alopecia-intellectual disability syndrome 2;

Symbol : APMR2;

CISMeF acronym : APMR2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Alopecia-mental retardation syndrome 2;

Description : For a discussion of genetic heterogeneity of alopecia with mental retardation, see APMR1 (203650).;

Inheritance : Autosomal recessive;

Prefixed ID : %610422;

Details

Origin ID

610422;

UMLS CUI

C1835852;

Currated CISMeF NLP mapping
- Alopecia-Mental retardation syndrome 2 [MeSH concept]
- Alopecia-Mental retardation syndrome 2 [MeSH Supplementary Concept]
DO Cross reference
- alopecia-mental retardation syndrome 2 [DO Concept]
HPO term(s)
- Alopecia universalis [HPO term]
- Autosomal recessive inheritance [HPO term]
- Intellectual disability [HPO term]
ORDO concept(s)
- Alopecia-intellectual disability syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alopecia-Mental retardation syndrome 2 [MeSH Supplementary Concept]
- Alopecia-Mental retardation syndrome 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients