Otitis media, susceptibility to

Preferred Label : Otitis media, susceptibility to;

Symbol : OMS;

CISMeF acronym : COME/ROM; OMS;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Otitis media, chronic/recurrent; COME/ROM;

Inheritance : Autosomal dominant;

Molecular basis : Susceptibility conferred by mutation in the alpha-2-macroglobulin-like 1 gene (A2ML1, 610627.0004);

Prefixed ID : #166760;

Details

Origin ID

166760;

UMLS CUI

C1833692;

Automatic exact mappings (from CISMeF team)
- Opsoclonus-myoclonus syndrome [ORDO Disease]
- Premenstrual tension syndrome (disorder) [SNOMED CT concept]
- Recurrent otitis media [HPO term]
- World Health Organization [COVID-19 Thesaurus concept]
- World health organization [Artificial nutrition thesaurus concept]
- world health organization [MeSH Descriptor]
Currated CISMeF NLP mapping
- Susceptibility to otitis media [HPO term]
False automatic mappings
- Oman [NCIt concept]
Genes related to phenotype
- Alpha-2-macroglobulin-like 1 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Polygenic inheritance [HPO term]
- Recurrent otitis media [HPO term]
- Susceptibility to otitis media [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Susceptibility to otitis media [HPO term]

Keyword's position in hierarchy(ies) :

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