wolfram syndrome 2

Preferred Label : wolfram syndrome 2;

Origin ID

C565733;

UMLS CUI

C1858028;

CISMeF manual mappings
- Wolfram syndrome type 2 [Disease (Nov.)]
Currated CISMeF NLP mapping
- Wolfram syndrome 2 [DO Concept]
- Wolfram syndrome 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- aging, premature [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
- mitochondrial diseases [MeSH Descriptor]
- optic atrophy [MeSH Descriptor]
Record concept(s)
- wolfram syndrome 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Wolfram syndrome 2 [OMIM Phenotype]
- Wolfram syndrome 2 [DO Concept]
- Wolfram syndrome type 2 [Disease (Nov.)]