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nonsyndromic genetic hearing loss

Go to external page http://purl.obolibrary.org/obo/MONDO_0019497

A disease characterized by hearing loss that is not part of a larger syndrome. [ MONDO : patterns/isolated ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:87884 (MONDO:equivalentTo)
  • MESH:C580334 (MONDO:equivalentTo)
  • EFO:0009076 (MONDO:equivalentTo)
  • DOID:0050563 (MONDO:equivalentTo)
  • UMLS:CN043648 (MONDO:equivalentTo)
  • GARD:0006410 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, ordo_group_of_disorders

definition
  • A disease characterized by hearing loss that is not part of a larger syndrome.
exactMatch
  • http://identifiers.org/mesh/C580334
  • http://purl.obolibrary.org/obo/DOID_0050563
  • http://linkedlifedata.com/resource/umls/id/CN043648
  • http://www.orpha.net/ORDO/Orphanet_87884
has broad synonym
  • nonsyndromic hearing loss
  • nonsyndromic deafness
has exact synonym
  • nonsyndromic hereditary hearing loss
has narrow synonym
  • isolated genetic deafness
  • non-syndromic genetic deafness
  • familial deafness
  • nonsyndromic genetic deafness
id
  • MONDO:0019497
seeAlso
  • https://rarediseases.info.nih.gov/diseases/6410/familial-deafness
term tracker item
  • https://github.com/monarch-initiative/mondo/issues/551