Retinitis pigmentosa 17

Preferred Label : Retinitis pigmentosa 17;

Symbol : RP17;

CISMeF acronym : RP17;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant (17);

Prefixed ID : #600852;

Details

Origin ID

600852;

UMLS CUI

C1833245;

Broader ORDO disease(s)
- Retinitis pigmentosa [ORDO Disease]
Currated CISMeF NLP mapping
- retinitis pigmentosa 17 [DO Concept]
- retinitis pigmentosa 17 [Disease (Nov.)]
- retinitis pigmentosa 17 [MeSH concept]
- retinitis pigmentosa 17 [MeSH Supplementary Concept]
DO Cross reference
- retinitis pigmentosa 17 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bone spicule pigmentation of the retina [HPO term]
- Color vision defect [HPO term]
- Nyctalopia [HPO term]
- Photophobia [HPO term]
- Rod-cone dystrophy [HPO term]
ORDO concept(s)
- Retinitis pigmentosa [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- retinitis pigmentosa 17 [MeSH Supplementary Concept]
- retinitis pigmentosa 17 [MeSH concept]
- retinitis pigmentosa 17 [DO Concept]
- retinitis pigmentosa 17 [Disease (Nov.)]

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