Retinitis pigmentosa 29

Preferred Label : Retinitis pigmentosa 29;

Symbol : RP29;

CISMeF acronym : RP29;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of retinitis pigmentosa, see 268000.;

Inheritance : Autosomal recessive;

Prefixed ID : %612165;

Details

Origin ID

612165;

UMLS CUI

C2677325;

Currated CISMeF NLP mapping
- retinitis pigmentosa 29 [DO Concept]
- retinitis pigmentosa 29 [MeSH concept]
- retinitis pigmentosa 29 [MeSH Supplementary Concept]
DO Cross reference
- retinitis pigmentosa 29 [DO Concept]
HPO term(s)
- Attenuation of retinal blood vessels [HPO term]
- Autosomal recessive inheritance [HPO term]
- Blindness [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 29 [MeSH Supplementary Concept]
- retinitis pigmentosa 29 [MeSH concept]
- retinitis pigmentosa 29 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients