macular dystrophy, retinal, 1, north carolina type

Preferred Label : macular dystrophy, retinal, 1, north carolina type;

MeSH synonym : retinal pigment epithelial dystrophy, central; north carolina macular dystrophy; central areolar pigment epithelial dystrophy; foveal dystrophy, progressive;

Details

Origin ID

C537835;

UMLS CUI

C0730294;

Automatic exact mappings (from CISMeF team)
- obsolete Foveal dystrophy [HPO term]
CISMeF manual mappings
- North Carolina macular dystrophy [ORDO Disease]
Currated CISMeF NLP mapping
- Macular Dystrophy, Retinal, 1 [NCIt concept]
- Macular dystrophy, retinal, 1, north carolina type [OMIM Phenotype]
- North Carolina macular dystrophy [ICD-11 More detail]
- North Carolina macular dystrophy (disorder) [SNOMED CT concept]
- Progressive foveal dystrophy [HPO term]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
ORDO relation(s)
- North Carolina macular dystrophy [ORDO Disease]
Record concept(s)
- Macular dystrophy, retinal, 1, North Carolina type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Macular Dystrophy, Retinal, 1 [NCIt concept]
- Macular dystrophy, retinal, 1, north carolina type [OMIM Phenotype]
- North Carolina macular dystrophy [ORDO Disease]
- North Carolina macular dystrophy (disorder) [SNOMED CT concept]
- Progressive foveal dystrophy [HPO term]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients