Retinopathy, pericentral pigmentary, dominant

Preferred Label : Retinopathy, pericentral pigmentary, dominant;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 180210;

Details

Origin ID

180210;

UMLS CUI

C1867261;

Currated CISMeF NLP mapping
- dominant pericentral pigmentary retinopathy [DO Concept]
- retinopathy, pericentral pigmentary, dominant [MeSH concept]
- retinopathy, pericentral pigmentary, dominant [MeSH Supplementary Concept]
DO Cross reference
- dominant pericentral pigmentary retinopathy [DO Concept]
HPO term(s)
- Attenuation of retinal blood vessels [HPO term]
- Autosomal dominant inheritance [HPO term]
- Blindness [HPO term]
- Bone spicule pigmentation of the retina [HPO term]
- Nyctalopia [HPO term]
- Pigmentary retinopathy [HPO term]
- Retinal atrophy [HPO term]
- Retinal dystrophy [HPO term]
- Retinopathy [HPO term]
ORDO concept(s)
- Retinitis pigmentosa [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- dominant pericentral pigmentary retinopathy [DO Concept]
- retinopathy, pericentral pigmentary, dominant [MeSH Supplementary Concept]
- retinopathy, pericentral pigmentary, dominant [MeSH concept]

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