Choroidal dystrophy, central areolar, 3

Preferred Label : Choroidal dystrophy, central areolar, 3;

Symbol : CACD3;

CISMeF acronym : CACD3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Choroidal dystrophy, central areolar, with or without drusen;

Description : For a general phenotypic description and discussion of genetic heterogeneity of central areolar choroidal dystrophy, see CACD1 (215500).;

Inheritance : Autosomal dominant;

Prefixed ID : %613144;

Details

Origin ID

613144;

UMLS CUI

C2751055;

Currated CISMeF NLP mapping
- choroidal dystrophy, central areolar 3 [MeSH concept]
- choroidal dystrophy, central areolar 3 [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Chorioretinal atrophy [HPO term]
- Drusen [HPO term]
ORDO concept(s)
- Central areolar choroidal dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- choroidal dystrophy, central areolar 3 [MeSH Supplementary Concept]
- choroidal dystrophy, central areolar 3 [MeSH concept]
Validated automatic mappings to NTBT
- Central areolar choroidal dystrophy [ORDO Disease]

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