Hearing loss associated with syndrome

Code	`232333009`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20020131

718574003Abruzzo Erickson syndrome disorder

1299152003Adult-onset progressive leucoencephalopathy, early-onset deafness disorder

720517001Ataxia with deafness and intellectual disability syndrome disorder

720518006Athabaskan brainstem dysgenesis syndrome disorder

720519003Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome disorder

1222649004Auditory neuropathy, optic atrophy syndrome disorder

1229999001Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome disorder

1204415006Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome disorder

10170007Black locks, oculocutaneous albinism, AND deafness of the sensorineural type disorder

720567008Bosley Salih Alorainy syndrome disorder

764810000Branchiootic syndrome disorder

1332382002COMMAD syndrome disorder

720601000Camptodactyly and tall stature with scoliosis and hearing loss syndrome disorder

1220595008Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome disorder

726621009Caudal appendage deafness syndrome disorder

726669007Central nervous system calcification, deafness, tubular acidosis, anaemia syndrome disorder

720634003Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome disorder

763136000Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome disorder

1281843005Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome disorder

717761005Choroideraemia with deafness and obesity syndrome disorder

773610007Chudley McCullough syndrome disorder

720639008Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome disorder

719102004Congenital cataract with ataxia and deafness syndrome disorder

722378009Congenital cataract with deafness and hypogonadism syndrome disorder

773648002Congenital cataract, hearing loss, severe developmental delay syndrome disorder

702360007Congenital deafness with labyrinthine aplasia, microtia and microdontia disorder

720749004Congenital hereditary endothelial dystrophy and perceptive deafness syndrome disorder

732248005Coxoauricular syndrome disorder

1172604004DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome disorder

721084001Deaf blind hypopigmentation syndrome Yemenite type disorder

718714006Deafness and hypogonadism syndrome disorder

721087008Deafness and intellectual disability Martin Probst type syndrome disorder

720506002Deafness and myopia syndrome disorder

716245003Deafness craniofacial syndrome disorder

773735007Deafness with onychodystrophy syndrome disorder

721085000Deafness, enamel hypoplasia, nail defect syndrome disorder

763688008Deafness, encephaloneuropathy, obesity, valvulopathy syndrome disorder

721086004Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome disorder

733071009Deafness, small bowel diverticulosis, neuropathy syndrome disorder

733069009Deafness, vitiligo, achalasia syndrome disorder

721089006Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome disorder

721092005Developmental malformation, deafness, dystonia syndrome disorder

720515009Distal arthrogryposis type 6 disorder

1230014007Duane retraction syndrome with congenital deafness disorder

733050004Dysmorphism, short stature, deafness, disorder of sex development syndrome disorder

1169356004Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome disorder

732953008Ectodermal dysplasia and sensorineural deafness syndrome disorder

720859009Ehlers-Danlos syndrome kyphoscoliotic and deafness type disorder

766870005Epiphyseal dysplasia, hearing loss, dysmorphism syndrome disorder

720955004Fine Lubinsky syndrome disorder

720957007Fountain syndrome disorder

782690007Gemignani syndrome disorder

722449007Gingival fibromatosis with progressive deafness syndrome disorder

721221000Hirschsprung disease with deafness and polydactyly syndrome disorder

773667003Hypertelorism, preauricular sinus, punctual pits, deafness syndrome disorder

773665006Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome disorder

724282009Hypoparathyroidism, deafness, renal disease syndrome disorder

239059004KID syndrome disorder

763774001Keipert syndrome disorder

1271009Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome disorder

721973006Lipodystrophy, intellectual disability, deafness syndrome disorder

766249007Lowe Kohn Cohen syndrome disorder

716007007Lowry Yong syndrome disorder

722035007MEDNIK syndrome disorder

724173009Maternally inherited cardiomyopathy and hearing loss syndrome disorder

733419006Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome disorder

1254651003Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome disorder

1300194008Mitchell syndrome disorder

732951005Mitochondrial myopathy, lactic acidosis, deafness syndrome disorder

733065003Myoclonus, cerebellar ataxia, deafness syndrome disorder

716170005Nathalie syndrome disorder

724093004Nephropathy, deafness, hyperparathyroidism syndrome disorder

724092009Nephrosis, deafness, urinary tract, digital malformation syndrome disorder

773647007Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome disorder

725137007Neutropenia, monocytopenia, deafness syndrome disorder

262764000Noise-induced permanent threshold shift disorder

770944002Oculootodental syndrome disorder

722019000Oculootoradial syndrome disorder

1222655009Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome disorder

1228871002PCNA-related progressive neurodegenerative photosensitivity syndrome disorder

723497003Peripheral neuropathy with sensorineural hearing impairment syndrome disorder

782752005Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome disorder

715506001Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome disorder

723452007Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome disorder

719272007Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome disorder

723504000Ramos Arroyo syndrome disorder

782942003Renal caliceal diverticuli and deafness syndrome disorder

724001005Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome disorder

186570004Rubella deafness disorder

1367656002SLC12A2-related developmental delay, intellectual disability, sensorineural deafness syndrome disorder

723993005Sensorineural deafness with dilated cardiomyopathy syndrome disorder

722213009Severe X-linked intellectual disability Gustavson type 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

723611008Split hand, split foot malformation with sensorineural hearing loss syndrome disorder

1172635005Split-foot malformation, mesoaxial polydactyly syndrome disorder

718763005Spondyloepiphyseal dysplasia MacDermot type disorder

719305006Stapes ankylosis with broad thumb and toe syndrome disorder

783097004Stickler syndrome type 3 disorder

47434006Waardenburg syndrome disorder

734022008Wolfram-like syndrome disorder

719838008X-linked hereditary sensory and autonomic neuropathy with deafness disorder

Hearing loss associated with syndrome

Synonyms

Parents (1)

Children (103)