Congenital sensorineural hearing loss (disorder)
| Code | 700453005 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | defined |
| Effective time | 20190731 |
95827002Congenital hearing disorder
disorder
60700002Sensorineural hearing loss
disorder
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disorder
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disorder
700112007Bartter syndrome type 4
disorder
67817003Björnstad syndrome
disorder
10170007Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
disorder
720567008Bosley Salih Alorainy syndrome
disorder
1332382002COMMAD syndrome
disorder
763136000Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
disorder
716238003Chitty Hall Baraitser syndrome
disorder
722378009Congenital cataract with deafness and hypogonadism syndrome
disorder
773648002Congenital cataract, hearing loss, severe developmental delay syndrome
disorder
773398005Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
disorder
1234911006Congenital cochleovestibular malformation
disorder
737377004Congenital mixed conductive and sensorineural hearing loss
disorder
702362004Craniofacial deafness hand syndrome
disorder
721087008Deafness and intellectual disability Martin Probst type syndrome
disorder
715527006Deafness and oligodontia syndrome
disorder
773735007Deafness with onychodystrophy syndrome
disorder
733071009Deafness, small bowel diverticulosis, neuropathy syndrome
disorder
766870005Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
disorder
720957007Fountain syndrome
disorder
93466004Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
disorder
773665006Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
disorder
373905003Jervell and Lange-Nielsen syndrome
disorder
763774001Keipert syndrome
disorder
1271009Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome
disorder
716007007Lowry Yong syndrome
disorder
711409002MEGDEL syndrome
disorder
773406003Mandibular hypoplasia, deafness, progeroid 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
232302007Mondini defect
disorder
24559001Mutilating keratoderma
disorder
733065003Myoclonus, cerebellar ataxia, deafness syndrome
disorder
770944002Oculootodental syndrome
disorder
1228871002PCNA-related progressive neurodegenerative photosensitivity syndrome
disorder
70348004Pendred's syndrome
disorder
765325002Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
disorder
236529001Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness
disorder
782942003Renal caliceal diverticuli and deafness syndrome
disorder
57838006Retinitis pigmentosa-deafness syndrome
disorder
186570004Rubella deafness
disorder
770751003Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
disorder
1284851009Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome
disorder
733089005Spastic paraplegia, nephritis, deafness syndrome
disorder
1172635005Split-foot malformation, mesoaxial polydactyly syndrome
disorder
783097004Stickler syndrome type 3
disorder
1260133007Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
disorder
777998000Temtamy preaxial brachydactyly syndrome
disorder
715952000Waardenburg Shah syndrome
disorder
237918004Waardenburg syndrome type 3
disorder
79665007Wildervanck syndrome
disorder