Hyperopia, high

Preferred Label : Hyperopia, high;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive vs. pseudodominance;

Prefixed ID : 238950;

Details

Origin ID

238950;

UMLS CUI

C1855925;

Automatic exact mappings (from CISMeF team)
- High hypermetropia [HPO term]
- hyperopia [MeSH Descriptor]
- hyperopia [MeSH concept]
Currated CISMeF NLP mapping
- hyperopia, high [MeSH concept]
- hyperopia, high [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- High hypermetropia [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- High hypermetropia [HPO term]
- hyperopia, high [MeSH Supplementary Concept]
- hyperopia, high [MeSH concept]

Keyword's position in hierarchy(ies) :

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