Congenital anomaly of ear with impairment of hearing   111339003

SNOMED CT code


SNOMED code111339003
nameCongenital anomaly of ear with impairment of hearing
statusactive
date introduced2002-01-31
fully specified name(s)Congenital anomaly of ear with impairment of hearing (disorder)
synonymsCongenital anomaly of ear with impairment of hearing
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteEar structure   117590005
attributes - group2
InterpretsHearing   47078008
parents
children
  • Autosomal dominant aplasia and myelodysplasia   778006008
  • Bilateral microtia with deafness and cleft palate syndrome   717909004
  • Branchiogenic deafness syndrome   717944002
  • Branchiootic syndrome   764810000
  • Cardiospondylocarpofacial syndrome   720612000
  • Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome   1281843005
  • Congenital cochleovestibular malformation   1234911006
  • Congenital conductive hearing loss   737344003
  • Congenital deafness with labyrinthine aplasia, microtia and microdontia   702360007
  • Congenital malformation of left ear with impairment of hearing   15984471000119107
  • Congenital malformation of right ear with impairment of hearing   15984431000119109
  • Coxoauricular syndrome   732248005
  • Deafness, vitiligo, achalasia syndrome   733069009
  • Earpit syndrome   232335002
  • Mondini defect   232302007
  • Neutropenia, monocytopenia, deafness syndrome   725137007
  • Pendred's syndrome   70348004
  • Sellars Beighton syndrome   716243005
  • Sinoatrial node dysfunction and deafness   770784003
  • Stapes ankylosis with broad thumb and toe syndrome   719305006
  • Thickened earlobe with conductive deafness syndrome   722476007
  • X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome   1167372000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Congenital anomaly of ear with impairment of hearing   111339003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of sensory organ   1279550006
        Disorder of ear   25906001
          Congenital malformation of ear   275259005
            Congenital anomaly of ear with impairment of hearing   111339003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Congenital anomaly of ear with impairment of hearing   111339003

ancestors
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