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Wolfram-like syndrome

^ http://purl.obolibrary.org/obo/MONDO_0013673


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 ]

Term info

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

ordo_disease

abbreviation
WFSL [ OMIM:614296 MONDO:Lexical ]

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, https://omim.org/entry/614296, http://linkedlifedata.com/resource/umls/id/C4518338, http://purl.obolibrary.org/obo/Orphanet_411590, http://identifiers.org/mesh/C565631

has exact synonym

Wolfram-like syndrome

has related synonym

WFSL, Wolfram-like syndrome, autosomal dominant, hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation

id

MONDO:0013673