Rod-Cone dystrophy, sensorineural deafness, and Fanconi-Type renal dysfunction

Preferred Label : Rod-Cone dystrophy, sensorineural deafness, and Fanconi-Type renal dysfunction;

Origin ID

C564829;

UMLS CUI

C1849333;

Currated CISMeF NLP mapping
- Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction [OMIM Phenotype]
MeSH term(s) associated for indexing
- fanconi syndrome [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- Rod-Cone dystrophy, sensorineural deafness, and Fanconi-Type renal dysfunction [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction [OMIM Phenotype]