Macular dystrophy, vitelliform, 1

Preferred Label : Macular dystrophy, vitelliform, 1;

Symbol : VMD1;

CISMeF acronym : VMD1;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Macular dystrophy, atypical vitelliform;

Inheritance : Autosomal dominant;

Prefixed ID : %153840;

Details

Origin ID

153840;

UMLS CUI

C4551953;

Currated CISMeF NLP mapping
- Atypical vitelliform macular dystrophy [HPO term]
- Macular dystrophy, atypical vitelliform [MeSH concept]
- macular dystrophy, atypical vitelliform [MeSH Supplementary Concept]
DO Cross reference
- vitelliform macular dystrophy [DO Concept]
HPO term(s)
- Atypical vitelliform macular dystrophy [HPO term]
- Autosomal dominant inheritance [HPO term]
- Late onset [HPO term]
- Macular dystrophy [HPO term]
- Reduced visual acuity [HPO term]
- Visual field defect [HPO term]
- Visual impairment [HPO term]
- Vitelliform-like macular lesions [HPO term]
ORDO concept(s)
- Adult-onset foveomacular vitelliform dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atypical vitelliform macular dystrophy [HPO term]
- Macular dystrophy, atypical vitelliform [MeSH concept]
- macular dystrophy, atypical vitelliform [MeSH Supplementary Concept]

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