Hearing loss
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Hearing loss associated with syndrome (disorder)
Hearing loss associated with syndrome
Syndromal deafness
gehoorverlies bij syndroom
Id232333009
StatusPrimitive
Finding siteStructure of auditory system
InterpretsHearing
ICD-10 complex map reference set
TargetH91.8
RuleTRUE
AdviceALWAYS H91.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
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Abruzzo Erickson syndrome
Ataxia with deafness and intellectual disability syndrome
Athabaskan brainstem dysgenesis syndrome
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
Auditory neuropathy, optic atrophy syndrome
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
Bosley Salih Alorainy syndrome
Branchiootic syndrome
Camptodactyly and tall stature with scoliosis and hearing loss syndrome
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
Caudal appendage deafness syndrome
Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
Choroideremia with deafness and obesity syndrome
Chudley McCullough syndrome
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome
Congenital cataract with ataxia and deafness syndrome
Congenital cataract with deafness and hypogonadism syndrome
Congenital cataract, hearing loss, severe developmental delay syndrome
Congenital deafness with labyrinthine aplasia, microtia and microdontia
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome
Coxoauricular syndrome
Deaf blind hypopigmentation syndrome Yemenite type
Deafness and hypogonadism syndrome
Deafness and intellectual disability Martin Probst type syndrome
Deafness and myopia syndrome
Deafness craniofacial syndrome
Deafness with onychodystrophy syndrome2
Deafness, enamel hypoplasia, nail defect syndrome
Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
Deafness, small bowel diverticulosis, neuropathy syndrome
Deafness, vitiligo, achalasia syndrome
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
Developmental malformation, deafness, dystonia syndrome
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
Distal arthrogryposis type 6
Duane retraction syndrome with congenital deafness
Dysmorphism, short stature, deafness, disorder of sex development syndrome
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome
Ectodermal dysplasia and sensorineural deafness syndrome
Ehlers-Danlos syndrome kyphoscoliotic and deafness type
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
Fine Lubinsky syndrome
Fountain syndrome
Gemignani syndrome
Gingival fibromatosis with progressive deafness syndrome
Hirschsprung disease with deafness and polydactyly syndrome
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
Hypoparathyroidism, deafness, renal disease syndrome
Keipert syndrome
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome
Lipodystrophy, intellectual disability, deafness syndrome
Lipodystrophy, intellectual disability, deafness syndrome
Lowe Kohn Cohen syndrome
Lowry Yong syndrome
Maternally inherited cardiomyopathy and hearing loss syndrome
MEDNIK syndrome
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome
Mitochondrial myopathy, lactic acidosis, deafness syndrome
Myoclonus, cerebellar ataxia, deafness syndrome
Nathalie syndrome
Nephropathy, deafness, hyperparathyroidism syndrome
Nephrosis, deafness, urinary tract, digital malformation syndrome
Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome
Neutropenia, monocytopenia, deafness syndrome
Noise-induced permanent threshold shift
Oculootodental syndrome
Oculootoradial syndrome
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
PCNA-related progressive neurodegenerative photosensitivity syndrome
Peripheral neuropathy with sensorineural hearing impairment syndrome
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
Ramos Arroyo syndrome
Renal caliceal diverticuli and deafness syndrome
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
Rubella deafness
Sensorineural deafness with dilated cardiomyopathy syndrome
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
Severe X-linked intellectual disability Gustavson type
Spastic paraplegia, nephritis, deafness syndrome
Split hand, split foot malformation with sensorineural hearing loss syndrome
Split-foot malformation, mesoaxial polydactyly syndrome
Spondyloepiphyseal dysplasia MacDermot type
Stapes ankylosis with broad thumb and toe syndrome
Stickler syndrome type 3
Waardenburg's syndrome5
Wolfram-like syndrome
X-linked hereditary sensory and autonomic neuropathy with deafness