Retinal dystrophy, reticular pigmentary, of posterior pole

Preferred Label : Retinal dystrophy, reticular pigmentary, of posterior pole;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 267800;

Details

Origin ID

267800;

UMLS CUI

C1849407;

Currated CISMeF NLP mapping
- retinal dystrophy, reticular pigmentary, of posterior pole [MeSH concept]
- retinal dystrophy, reticular pigmentary, of posterior pole [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Drusen [HPO term]
- Reticular pigmentary degeneration [HPO term]
- Retinal dystrophy [HPO term]
ORDO concept(s)
- Reticular dystrophy of the retinal pigment epithelium [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- retinal dystrophy, reticular pigmentary, of posterior pole [MeSH Supplementary Concept]
- retinal dystrophy, reticular pigmentary, of posterior pole [MeSH concept]

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