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LD2H.Y Other specified syndromic genetic deafness

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Other specified syndromic genetic deafness
• Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness
• ABCD - [Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness] syndrome
• Albinism-deafness syndrome
• Alström syndrome
• Ataxia - deafness - intellectual disability syndrome
• Athabaskan brainstem dysgenesis syndrome
• Atherosclerosis - deafness - diabetes - epilepsy - nephropathy
• Bilateral microtia - deafness - cleft palate
• Bosley-Salih-Alorainy syndrome
• Brown-Vialetto-van Laere syndrome
• Sensorineural hearing loss - pontobulbar palsy
• Cataract - ataxia - deafness
• Cataract - deafness - hypogonadism
• Caudal appendage - deafness
• Central nervous system calcification - deafness - tubular acidosis - anaemia
• Choanal atresia - deafness - cardiac defects - dysmorphism
• Choroideremia - deafness - obesity
• Cleft lip or palate - deafness - sacral lipoma
• Cochleosaccular degeneration - cataract
• Corneal anaesthesia - deafness - intellectual disability
• Corneal dystrophy - perceptive deafness
• Craniofacial-deafness-hand syndrome
• Deaf blind hypopigmentation syndrome, Yemenite type
• Deafness - craniofacial syndrome
• Deafness - epiphyseal dysplasia - short stature
• Deafness - genital anomalies - metacarpal and metatarsal synostosis
• Deafness - hypogonadism
• Deafness - intellectual deficit syndrome, Martin-Probst type
• Martin-Probst syndrome
• Deafness - oligodontia
• Deafness - peripheral neuropathy - arterial disease
• Deafness - skeletal dysplasia - lip granuloma
• Fountain syndrome
• Deafness - small bowel diverticulosis - neuropathy
• Deafness - vitiligo - achalasia
• Deafness-infertility syndrome
• 15q15.3 deletion syndrome
• Monosomy 15q15.3
• 15q15.3 deletion
• Dentinogenesis imperfecta - short stature - hearing loss - intellectual deficit
• Developmental delay - deafness, Hildebrand type
• Developmental malformations - deafness - dystonia
• Ermine phenotype
• Gingival fibromatosis - progressive deafness
• Hearing loss - familial salivary gland insensitivity to aldosterone
• Hirschsprung disease - deafness - polydactyly
• Hypospadias-hypertelorism-coloboma and deafness
• Iris dysplasia - hypertelorism - deafness
• Lethal ataxia with deafness and optic atrophy
• Arts syndrome
• Lipodystrophy - intellectual deficit - deafness
• Lowe-Kohn-Cohen syndrome
• Deafness - nephritis - anorectal malformation
• Maternally inherited diabetes and deafness
• Mitochondrial diabetes
• Maxillonasal dysplasia
• Intellectual disability – enteropathy – deafness – neuropathy – ichthyosis – keratoderma syndrome
• Mental retardation – enteropathy – deafness – neuropathy – ichthyosis – keratoderma syndrome
• MEDNIK - [Mental retardation – enteropathy – deafness – neuropathy – ichthyosis – keratoderma] syndrome
• Microcephaly - deafness - intellectual disability
• Microdontia - microtia type I - deafness
• Deafness with labyrinthine aplasia, microtia, and microdontia
• Mitral regurgitation - deafness - skeletal anomalies
• Myoclonus - cerebellar ataxia - deafness
• N syndrome
• Nephropathy - deafness - hyperparathyroidism
• Nephrosis - deafness - urinary tract - digital malformations
• Neutropaenia - monocytopaenia - deafness
• Olivopontocerebellar atrophy - deafness
• Osteochondrodysplatic nanism - deafness - retinitis pigmentosa
• Peripheral neuropathy, Fiskerstrand type
• Perrault syndrome
• Phocomelia - ectrodactyly - deafness - sinus arrhythmia
• Hypertrophic cardiomyopathy due to Kearns–Sayre syndrome
• progressive sensorineural hearing loss - hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy associated with progressive sensorineural hearing loss
• Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism
• Richards-Rundle syndrome
• Schizophrenia - intellectual disability - deafness - retinitis
• Sensorineural hearing loss - early greying - essential tremor
• SeSAME syndrome
• EAST syndrome
• Short stature - deafness - neutrophil dysfunction - dysmorphism
• Spastic paraparesis - deafness
• Split hand - split foot - deafness
• Thickened earlobes - conductive deafness
• Deafness - optic atrophy syndrome
• Optic atrophy, deafness, ophthalmoplegia, myopathy
• Autosomal dominant optic atrophy and congenital deafness
• Ocular albinism - late-onset sensorineural deafness
• Spastic paraplegia - nephritis - deafness
• Metaphyseal dysostosis - intellectual deficit - conductive deafness
• Knuckle pads – leukonychia – sensorineural deafness
• Bart-Pumphrey syndrome (MIM 149200)
• Alport syndrome
• Alport syndrome, autosomal dominant
• Alport syndrome, autosomal recessive
• Alport syndrome, X-linked
• Alport syndrome, X-linked diffuse leiomyomatosis
• Cardioauditory syndrome

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