doyne honeycomb retinal dystrophy

Preferred Label : doyne honeycomb retinal dystrophy;

CISMeF synonym : malattia leventinese;

MeSH synonym : doyne honeycomb degeneration of retina; Malattia Leventinese; Drusen, Radial, Autosomal Dominant;

Details

Origin ID

C535602;

UMLS CUI

C1832174;

Currated CISMeF NLP mapping
- Dominant drusen (disorder) [SNOMED CT concept]
- Doyne honeycomb retinal dystrophy [DO Concept]
- Doyne honeycomb retinal dystrophy [OMIM Phenotype]
- Familial drusen [ICD-11 More detail]
- Familial drusen [ORDO Disease]
- Malattia Leventinese [ICD-11 More detail]
- Malattia leventinese [Disease (Nov.)]
DO Cross reference
- Doyne honeycomb retinal dystrophy [DO Concept]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
- optic disk drusen [MeSH Descriptor]
Record concept(s)
- Doyne honeycomb retinal dystrophy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dominant drusen (disorder) [SNOMED CT concept]
- Doyne honeycomb retinal dystrophy [OMIM Phenotype]
- Doyne honeycomb retinal dystrophy [DO Concept]

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