newfoundland Rod-Cone dystrophy

Preferred Label : newfoundland Rod-Cone dystrophy;

MeSH note : RLBP1 protein, human mutation;

Origin ID

C564391;

UMLS CUI

C1843815;

Currated CISMeF NLP mapping
- Newfoundland cone-rod dystrophy [DO Concept]
- Newfoundland rod-cone dystrophy [OMIM Phenotype]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- newfoundland Rod-Cone dystrophy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Newfoundland cone-rod dystrophy [DO Concept]
- Newfoundland rod-cone dystrophy [OMIM Phenotype]