SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Sex-linked hereditary disorder  82852009

X-linked hereditary disease  128430005

X-linked sensorineural hearing loss   232329002

SNOMED CT code


SNOMED code232329002
nameX-linked sensorineural hearing loss
statusactive
date introduced2002-01-31
fully specified name(s)X-linked sensorineural hearing loss (disorder)
synonymsX-linked sensorineural hearing loss
attributes - group2
Finding siteAuditory structure   91159003
attributes - group1
InterpretsHearing   47078008
Has interpretationImpaired   260379002
parents
children
  • Abruzzo Erickson syndrome   718574003
  • Alport syndrome X-linked   717768004
  • Choroideremia with deafness and obesity syndrome   717761005
  • Deafness and intellectual disability Martin Probst type syndrome   721087008
  • Ocular albinism with late-onset sensorineural deafness   722054007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked sensorineural hearing loss   232329002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Ear and auditory finding   118236001
      Disorder of auditory system   362966006
        Auditory system hereditary disorder   362991006
          X-linked sensorineural hearing loss   232329002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Sensorineural hearing loss   60700002
              X-linked sensorineural hearing loss   232329002

ancestors
sorted most to least specific
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