Decreased hearing (finding)
| Code | 103276001 |
|---|---|
| Semantic tag | finding |
| Module | international |
| Definition | defined |
| Effective time | 20080731 |
154091000119106Decline in functional status
finding
118230007Hearing finding
finding
1299152003Adult-onset progressive leucoencephalopathy, early-onset deafness
disorder
722285005Albinism with deafness syndrome
disorder
63702009Alstrom syndrome
disorder
1222649004Auditory neuropathy, optic atrophy syndrome
disorder
1229999001Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
disorder
733029008Autosomal dominant spastic paraplegia type 29
disorder
1204415006Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
disorder
238047006Beta-D-mannosidosis
disorder
1332382002COMMAD syndrome
disorder
1281843005Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
disorder
1234911006Congenital cochleovestibular malformation
disorder
737344003Congenital conductive hearing loss
disorder
702360007Congenital deafness with labyrinthine aplasia, microtia and microdontia
disorder
1197059004Congenital ichthyosis, microcephalus, tetraplegia syndrome
disorder
715527006Deafness and oligodontia syndrome
disorder
773735007Deafness with onychodystrophy syndrome
disorder
721085000Deafness, enamel hypoplasia, nail defect syndrome
disorder
1230014007Duane retraction syndrome with congenital deafness
disorder
162340000Hearing difficulty
finding
300227009Hearing for voice impaired
finding
722453009Hennekam Beemer syndrome
disorder
1260450002Infantile multisystem neurologic, endocrine, pancreatic disease
disorder
239059004KID syndrome
disorder
237617006Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
disorder
1254651003Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome
disorder
1300194008Mitchell syndrome
disorder
1217379007NKX6-2-related autosomal recessive hypomyelinating leucodystrophy
disorder
1260199008Non-syndromic genetic hearing loss
disorder
1222655009Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
disorder
1237343009Otodental syndrome
disorder
1228871002PCNA-related progressive neurodegenerative photosensitivity syndrome
disorder
1237413006Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome
disorder
1367656002SLC12A2-related developmental delay, intellectual disability, sensorineural deafness syndrome
disorder
1284851009Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome
disorder
733089005Spastic paraplegia, nephritis, deafness syndrome
disorder
1356736002Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome
disorder
783097004Stickler syndrome type 3
disorder
1260133007Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
disorder
1255271005Type 1 diabetes mellitus, central and peripheral neurodegeneration syndrome
disorder
47434006Waardenburg syndrome
disorder
70694009Wolfram syndrome
disorder