keratitis, hereditary - CISMeF

CISMeF

chu

Keratitis, hereditaryMeSH Supplementary Concept

Preferred Label : keratitis, hereditary;

MeSH synonym : dominantly inherited keratitis;

Details

Origin ID

C537022;

UMLS CUI

C1835698;

Currated CISMeF NLP mapping
- Autosomal dominant keratitis (disorder) [SNOMED CT concept]
- Keratitis, hereditary [OMIM Phenotype]
- autosomal dominant keratitis [DO Concept]
- hereditary keratitis [Disease (Nov.)]
DO Cross reference
- autosomal dominant keratitis [DO Concept]
Has phenotype(s) (HPO)
- Hereditary childhood corneal clouding [HPO term]
MeSH term(s) associated for indexing
- keratitis [MeSH Descriptor]
ORDO relation(s)
- Autosomal dominant keratitis [ORDO Disease]
Record concept(s)
- Keratitis, hereditary [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant keratitis [ORDO Disease]
- Autosomal dominant keratitis (disorder) [SNOMED CT concept]
- Keratitis, hereditary [OMIM Phenotype]
- autosomal dominant keratitis [DO Concept]
Validated automatic mappings to BTNT
- Autosomal dominant keratitis [ORDO Disease]

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25/05/2025

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