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)
- dystrophies primarily involving Bruch's membrane (H31.1-)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- diabetes mellitus related eye conditions (E09.3-, E10.3-, E11.3-, E13.3-)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury (trauma) of eye and orbit (S05.-)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-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)
Also Known As / Clinical Terms
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
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.
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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.