Decline in functional status
Hearing finding
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Decreased hearing (finding)
Decreased hearing
Id103276001
StatusDefined
Has interpretationDecreased
InterpretsHearing
Finding siteStructure of auditory system
Global Patient Set
General Practice / Family Practice reference set
International Patient Summary
SNOMED CT to MedDRA simple map
SNOMED CT to ICD-10 extended map
TargetH93.2
RuleTRUE
AdviceALWAYS H93.2
CorrelationSNOMED CT source code to target map code correlation not specified
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Adult-onset progressive leukoencephalopathy, early-onset deafness
Albinism with deafness syndrome
Alstrom syndrome
Auditory neuropathy, optic atrophy syndrome
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
Autosomal dominant spastic paraplegia type 29
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
Beta-D-mannosidosis
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
COMMAD syndrome
Congenital cochleovestibular malformation
Congenital conductive hearing loss5
Congenital deafness with labyrinthine aplasia, microtia and microdontia
Congenital ichthyosis, microcephalus, tetraplegia syndrome
Deafness and oligodontia syndrome
Deafness with onychodystrophy syndrome2
Deafness, enamel hypoplasia, nail defect syndrome
Duane retraction syndrome with congenital deafness
Hearing difficulty5
Hearing for voice impaired4
Hennekam Beemer syndrome
Infantile multisystem neurologic, endocrine, pancreatic disease
KID syndrome2
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome
Mitchell syndrome
NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
Non-syndromic genetic hearing loss2
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
Otodental syndrome
PCNA-related progressive neurodegenerative photosensitivity syndrome
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome
SLC12A2-related developmental delay, intellectual disability, sensorineural deafness syndrome
Spastic paraplegia, nephritis, deafness syndrome
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome
Stickler syndrome type 3
Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
Type 1 diabetes mellitus, central and peripheral neurodegeneration syndrome
Waardenburg syndrome5
Wolfram syndrome2