Wolfram-like syndrome is a rare endocrine disease characterized by the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy. Psychiatric (i.e. anxiety, depression, hallucinations) and sleep disorders, the only neurologic abnormalities observed in this disease, have been reported in rare cases. Unlike Wolfram syndrome, patients with Wolfram-like syndrome do not report endocrine or cardiac findings. [ Orphanet:411590 ]

This is just here as a test because I lose it

Term information

database cross reference
  • EFO:0009063 (MONDO:equivalentTo)
  • Orphanet:411590 (OMIM:614296)
  • ICD10:E13.8 (Orphanet:411590)
  • OMIM:614296 (Orphanet:411590)
  • DOID:0080584 (MONDO:equivalentTo)
  • MESH:C565631 (MONDO:equivalentTo)
  • SCTID:734022008 (MONDO:equivalentTo)
  • UMLS:C4518338 (MONDO:equivalentTo)
  • UMLS:C3280358 (Orphanet:411590)
Subsets

ordo_disease

closeMatch

http://linkedlifedata.com/resource/umls/id/C1857286

definition

Wolfram-like syndrome is a rare endocrine disease characterized by the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy. Psychiatric (i.e. anxiety, depression, hallucinations) and sleep disorders, the only neurologic abnormalities observed in this disease, have been reported in rare cases. Unlike Wolfram syndrome, patients with Wolfram-like syndrome do not report endocrine or cardiac findings.

exactMatch

http://identifiers.org/snomedct/734022008

http://purl.obolibrary.org/obo/DOID_0080584

http://linkedlifedata.com/resource/umls/id/C3280358

http://identifiers.org/omim/614296

http://www.orpha.net/ORDO/Orphanet_411590

http://linkedlifedata.com/resource/umls/id/C4518338

http://identifiers.org/mesh/C565631

has related synonym

WFSL

Wolfram-like syndrome, autosomal dominant

hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation

id

MONDO:0013673