Macular dystrophy, fenestrated sheen type

Preferred Label : Macular dystrophy, fenestrated sheen type;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 153890;

Details

Origin ID

153890;

UMLS CUI

C1835173;

Currated CISMeF NLP mapping
- macular dystrophy, fenestrated sheen type [MeSH concept]
- macular dystrophy, fenestrated sheen type [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Macular dystrophy [HPO term]
- Slowly progressive macular dystrophy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- macular dystrophy, fenestrated sheen type [MeSH Supplementary Concept]
- macular dystrophy, fenestrated sheen type [MeSH concept]

Keyword's position in hierarchy(ies) :

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