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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 ]

Synonyms: nonsyndromic genetic hearing loss nonsyndromic hereditary hearing loss

This is just here as a test because I lose it

Term information

database cross reference
  • icd11.foundation:1154032108 (https://orcid.org/0000-0001-5208-3432)
  • GARD:19091 (MONDO:GARD)
  • MEDGEN:1830101 (MONDO:equivalentTo)
  • UMLS:C5680182 (MONDO:equivalentTo)
  • DOID:0050563 (MONDO:equivalentTo)
  • MESH:C580334 (MONDO:equivalentTo)
  • Orphanet:87884 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disorder, otar, disease_grouping, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/551

exactMatch

http://identifiers.org/medgen/1830101

http://purl.obolibrary.org/obo/DOID_0050563

http://www.orpha.net/ORDO/Orphanet_87884

http://identifiers.org/mesh/C580334

http://linkedlifedata.com/resource/umls/id/C5680182

has broad synonym

nonsyndromic deafness

nonsyndromic hearing loss

has narrow synonym

isolated genetic deafness

familial deafness

nonsyndromic genetic deafness

non-syndromic genetic deafness

id

MONDO:0019497

seeAlso

https://rarediseases.info.nih.gov/diseases/6410/familial-deafness