H35.52
BillablePigmentary retinal dystrophy
Pigmentary retinal dystrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Albipunctate retinal dystrophy
- Retinitis pigmentosa
- Tapetoretinal dystrophy
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •diabetes mellitus related eye conditions, , ,E09.3, E10.3, E11.3, E13.3
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury (trauma) of eye and orbitS05
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •syphilis related eye disorders, , ,A50.01, A50.3, A51.43, A52.71
- •diabetic retinal disorders, , , ,E08.311-E08.359, E09.311-E09.359, E10.311-E10.359, E11.311-E11.359, E13.311-E13.359
Related Codes(4)
Also Known As / Clinical Terms(236)
SNOMED CT
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- RP - Retinitis pigmentosa28835009
- Retinitis pigmentosa28835009
- Drusen of optic disc33629003
- Hyaline bodies of optic disc33629003
- Optic disc drusen33629003
- Optic nerve head drusen33629003
- Neurological muscle paresis41786007
- Neurological muscle weakness41786007
- Retinitis pigmentosa-deafness syndrome57838006
- Usher syndrome57838006
- Usher's syndrome57838006
- HMSN VII128204009
- HSMN VII128204009
- Hereditary motor and sensory neuropathy type VII128204009
- Hereditary motor and sensory neuropathy with retinitis pigmentosa128204009
- Hereditary motor and sensory neuropathy, type VII128204009
- Hereditary motor-sensory neuropathy with retinitis pigmentosa128204009
- Hereditary sensory-motor neuropathy, type VII128204009
- Spastic quadriplegia192965001
- Spastic tetraplegia192965001
- Tapetoretinal dystrophy193415008
- Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy230230002
- Pattern dystrophy of macula232051002
- Autosomal dominant retinitis pigmentosa232052009
- Autosomal recessive retinitis pigmentosa232053004
- X-linked retinitis pigmentosa232054005
- X-linked retinitis pigmentosa heterozygote232055006
- Furukawa Takagi Nakao syndrome237611007
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus237611007
- NARP (neurogenic muscle weakness, ataxia, retinitis pigmentosa) syndrome237984008
- NARP syndrome237984008
- Neurogenic muscle weakness, ataxia and retinitis pigmentosa237984008
- Retinal pigment deposits247141006
- Macular pigment deposit247146001
- Conorenal syndrome254092004
- Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome254092004
- Saldino-Mainzer dysplasia254092004
- Cataract in child399336001
- Childhood cataract399336001
- Juvenile cataract399336001
- Hereditary retinal dystrophy primarily involving retinal pigment epithelium698847000
- Inherited retinal dystrophy primarily involving retinal pigment epithelium698847000
- Primary ciliary dyskinesia and retinitis pigmentosa syndrome719282008
- Bork syndrome719910004
- Tricho-retino-dento-digital syndrome719910004
- Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome719910004
- Cholestasis with pigmentary retinopathy and cleft palate syndrome720636001
- Hardikar syndrome720636001
- Cecatto de Lima Pinheiro syndrome722062004
- Oculotrichodysplasia722062004
- PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome723452007
- PHARC syndrome723452007
- Peripheral neuropathy Fiskerstrand type723452007
- Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome723452007
- Spastic quadriplegia, retinitis pigmentosa, intellectual disability syndrome723621000
- Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome723621000
- RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome723999009
- RHYNS syndrome723999009
- Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome723999009
- Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome724001005
- Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome724001005
- Autosomal recessive posterior column ataxia and retinitis pigmentosa724065003
- Posterior column ataxia with retinitis pigmentosa syndrome724065003
- Butterfly-shaped pattern dystrophy725590001
- Butterfly-shaped pigment dystrophy725590001
- Butterfly-shaped pigmentary macular dystrophy725590001
- Chang Davidson Carlson syndrome733113002
- Hypogonadotropic hypogonadism retinitis pigmentosa syndrome733113002
- Autosomal recessive leukoencephalopathy, ischaemic stroke, retinitis pigmentosa syndrome771476007
- Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome771476007
- Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome778021002
- Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome778021002
- Brachydactyly, short stature, retinitis pigmentosa syndrome782914000
- Retinitis pigmentosa-deafness syndrome type 31010610007
- Usher syndrome type 31010610007
- Progressive weakness of muscle1137511009
- Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome1172605003
- Retinal dystrophy, juvenile cataract, short stature syndrome1220597000
- Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome1220597000
- PXE-like (pseudoxanthoma elasticum-like) syndrome with retinitis pigmentosa1220599002
- Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa1220599002
- Retinitis pigmentosa due to systemic disease1231663000
- Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome1237514002
- Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome1237514002
- Body height below reference range1363478003
- MT-ATP6 mitochondrial disease1363509005
- Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial disease1363509005
- Hereditary cerebellar atrophy431641000124107
- Infantile and/or juvenile cataract342291000119102
- Retinal dystrophy due to systemic disorder40121000119107
- Retinal pigment epithelial dystrophy342581000119102
- Retinitis pigmentosa of bilateral eyes15699281000119107
- Retinitis pigmentosa of both eyes15699281000119107
- Retinitis pigmentosa of left eye15699201000119104
- Retinitis pigmentosa of right eye15699241000119102
UMLS
- Albipunctate retinal dystrophyC4551633
- Lauber's diseaseC4551633
- Pigmentary retinal dystrophyC4551633
- Retinal pigmentary dystrophyC4551633
- fundus albipunctatusC4551633
- pigmentary retinal dystrophyC4551633
- Pigmentary RetinopathiesC0035334
- Pigmentary RetinopathyC0035334
- RETINITIS PIGMENTOSAC0035334
- RP - Retinitis pigmentosaC0035334
- Retinitis PigmentosaC0035334
- Retinitis pigmentosaC0035334
- Retinitis pigmentosa (RP)C0035334
- Retinitis pigmentosa (disorder)C0035334
- Retinopathies, PigmentaryC0035334
- Retinopathy, PigmentaryC0035334
- Tapetoretinal DegenerationC0035334
- Tapetoretinal DegenerationsC0035334
- Tapetoretinal degenerationC0035334
- pigmentary retinopathyC0035334
- retinitis pigmentosaC0035334
- Tapetoretinal dystrophyC0339523
- Tapetoretinal dystrophy (disorder)C0339523
Clinical Terms
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
- Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
- Brachydactyly, short stature, retinitis pigmentosa syndrome
- Primary ciliary dyskinesia and retinitis pigmentosa syndrome
- Genetic syndromes of diabetes mellitus
- RP - Retinitis pigmentosa
- Usher syndrome type 3
- retinitis pigmentosa
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
- Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
- Conorenal syndrome
- Hereditary motor and sensory neuropathy, type VII
- Retinal pigmentary dystrophy
- Bork syndrome
- Retinal pigment deposits
- Autosomal recessive posterior column ataxia and retinitis pigmentosa
- Lauber's disease
- Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome
- Retinal dystrophy, juvenile cataract, short stature syndrome
- Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome
- Cholestasis with pigmentary retinopathy and cleft palate syndrome
- Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome
- Usher syndrome
- Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome
- Retinitis pigmentosa of both eyes
- fundus albipunctatus
- Retinitis pigmentosa of left eye
- Saldino-Mainzer dysplasia
- NARP (neurogenic muscle weakness, ataxia, retinitis pigmentosa) syndrome
- Optic nerve head drusen
- Retinitis pigmentosa of bilateral eyes
- Autosomal dominant retinitis pigmentosa
- Tapetoretinal dystrophy (disorder)
- Hereditary motor and sensory neuropathy with retinitis pigmentosa
- Hereditary cerebellar atrophy
- Diabetes mellitus associated with genetic syndrome
- Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
- Butterfly-shaped pigmentary macular dystrophy
- PXE-like (pseudoxanthoma elasticum-like) syndrome with retinitis pigmentosa
- Juvenile cataract
- Hereditary motor-sensory neuropathy with retinitis pigmentosa
- X-linked retinitis pigmentosa
- Chang Davidson Carlson syndrome
- Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
- Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome
- Oculotrichodysplasia
- Pattern dystrophy of macula
- Hereditary motor and sensory neuropathy type VII
- Tricho-retino-dento-digital syndrome
- Peripheral neuropathy Fiskerstrand type
- Retinitis pigmentosa (RP)
- X-linked retinitis pigmentosa heterozygote
- Tapetoretinal degeneration
- Macular pigment deposit
- Hereditary retinal dystrophy primarily involving retinal pigment epithelium
- Tapetoretinal Degenerations
- Retinitis pigmentosa due to systemic disease
- Spastic tetraplegia
- Retinitis pigmentosa-deafness syndrome type 3
- RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome
- Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
- Hyaline bodies of optic disc
- HMSN VII
- PHARC syndrome
- Retinitis pigmentosa of right eye
- Retinopathy, Pigmentary
- Body height below reference range
- Retinopathies, Pigmentary
- Hardikar syndrome
- Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome
- HSMN VII
- Autosomal recessive retinitis pigmentosa
- Pigmentary Retinopathy
- Cecatto de Lima Pinheiro syndrome
- Neurological muscle weakness
- Usher's syndrome
- Posterior column ataxia with retinitis pigmentosa syndrome
- Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome
- Butterfly-shaped pigment dystrophy
- Retinal pigment epithelial dystrophy
- Pigmentary Retinopathies
- Autosomal recessive leukoencephalopathy, ischaemic stroke, retinitis pigmentosa syndrome
- Neurological muscle paresis
- Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome
- Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
- Butterfly-shaped pattern dystrophy
- Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome
- Retinal dystrophy due to systemic disorder
- Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
- Retinitis pigmentosa (disorder)
- Progressive weakness of muscle
- MT-ATP6 mitochondrial disease
- Hereditary sensory-motor neuropathy, type VII
- Drusen of optic disc
- Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial disease
- Tapetoretinal dystrophy
- Inherited retinal dystrophy primarily involving retinal pigment epithelium
- PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome
- NARP syndrome
- Infantile and/or juvenile cataract
- Furukawa Takagi Nakao syndrome
- Optic disc drusen
- Cataract in child
- Albipunctate retinal dystrophy
- Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome
- Spastic quadriplegia
- Neurogenic muscle weakness, ataxia and retinitis pigmentosa
- Spastic quadriplegia, retinitis pigmentosa, intellectual disability syndrome
- RHYNS syndrome
- Retinitis pigmentosa-deafness syndrome
- Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome
- Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome
- Childhood cataract
Frequently Asked Questions
What is the ICD-10 code for pigmentary retinal dystrophy?
The ICD-10-CM code for pigmentary retinal dystrophy is H35.52. The full clinical description is "Pigmentary retinal dystrophy". H35.52 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H35.52 mean?
ICD-10-CM code H35.52 represents “Pigmentary retinal dystrophy”. It is classified under Chapter 7: Diseases of the Eye and Adnexa and is a billable/specific code that can be used on a claim.
Is H35.52 a billable code?
Yes, H35.52 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H35.52 in?
H35.52 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What codes cannot be used with H35.52?
H35.52 has Excludes1 notes indicating codes that cannot be used together with it, including: dystrophies primarily involving Bruch's membrane (H31.1-).
What SNOMED CT codes does H35.52 map to?
H35.52 maps to 51 SNOMED CT concepts: 232052009, 771476007, 724065003, 232053004, 1363478003, and 46 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H35.52?
H35.52 is linked to 3 UMLS Concept Unique Identifiers: C4551633, C0035334, C0339523. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does H35.52 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like pigmentary retinal dystrophy affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of H35.52?
There is no direct ICD-11 mapping available for H35.52 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.