H35.53
BillableOther dystrophies primarily involving the sensory retina
Other dystrophies primarily involving the sensory retina
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Stargardt's disease
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(90)
SNOMED CT
- FFM - Fundus flavimaculatus47673003
- Fundus flavimaculatus47673003
- Retinitis pigmentosa-deafness syndrome57838006
- Usher syndrome57838006
- Usher's syndrome57838006
- Hallgren's syndrome73119000
- Retinitis pigmentosa-deafness-ataxia syndrome73119000
- Hyaline retinal dystrophy193409008
- Sorsby fundus dystrophy193410003
- Sorsby pseudoinflammatory fundus dystrophy193410003
- Sorsby's fundus dystrophy193410003
- Progressive rod dystrophy232056007
- Usher syndrome type 1232057003
- Usher syndrome type 2232058008
- Progressive cone dystrophy (without rod involvement)267613004
- Cone dystrophy312917007
- Rod dystrophy313003009
- Hereditary retinal dystrophy primarily involving sensory retina698848005
- Inherited retinal dystrophy primarily involving sensory retina698848005
- Bilateral degeneration of macula12239101000119100
- Macular degeneration of both eyes12239101000119100
- Bilateral fundus flavimaculatus of eyes15628611000119101
- Fundus flavimaculatus of bilateral eyes15628611000119101
- Fundus flavimaculatus of both eyes15628611000119101
- Dystrophy of sensory retina35531000119107
- Sensory retinal dystrophy35531000119107
- Fundus flavimaculatus of left eye15628571000119105
- Fundus flavimaculatus of right eye15628531000119107
- Usher syndrome type 1F514793471000119104
UMLS
- Degeneration, Stargardt MacularC0271093
- FFMC0271093
- FFM - Fundus flavimaculatusC0271093
- FUNDUS FLAVIMACULATUSC0271093
- Familial juvenile macular degeneration syndromeC0271093
- Fundus FlavimaculatusC0271093
- Fundus flavimaculatusC0271093
- Fundus flavimaculatus (disorder)C0271093
- Macular Degeneration, StargardtC0271093
- STARGARDT DISEASEC0271093
- STGDC0271093
- Stargardt DiseaseC0271093
- Stargardt Macular DegenerationC0271093
- Stargardt Macular DegenerationsC0271093
- Stargardt diseaseC0271093
- Stargardt macular degenerationC0271093
- Stargardt's diseaseC0271093
- Stargardt's disease (disorder)C0271093
- fundus flavimaculatusC0271093
- stargardt's diseaseC0271093
- Other dystrophies primarily involving the sensory retinaC0154864
Clinical Terms
- STARGARDT DISEASE
- Hereditary retinal dystrophy primarily involving sensory retina
- Fundus flavimaculatus of right eye
- Fundus flavimaculatus (disorder)
- Stargardt's disease
- Retinitis pigmentosa-deafness-ataxia syndrome
- Fundus flavimaculatus of bilateral eyes
- Sorsby pseudoinflammatory fundus dystrophy
- FFM - Fundus flavimaculatus
- FFM
- Sorsby's fundus dystrophy
- Dystrophy of sensory retina
- Cone dystrophy
- Sorsby fundus dystrophy
- Progressive cone dystrophy (without rod involvement)
- Macular degeneration of both eyes
- FUNDUS FLAVIMACULATUS
- Stargardt's disease (disorder)
- Progressive rod dystrophy
- Rod dystrophy
- Usher syndrome type 2
- Stargardt Macular Degeneration
- Usher syndrome type 1F
- Familial juvenile macular degeneration syndrome
- Usher syndrome
- Bilateral degeneration of macula
- Fundus flavimaculatus of both eyes
- Usher syndrome type 1
- Inherited retinal dystrophy primarily involving sensory retina
- Macular Degeneration, Stargardt
- Fundus flavimaculatus of left eye
- Stargardt Macular Degenerations
- Usher's syndrome
- Hallgren's syndrome
- Retinitis pigmentosa-deafness syndrome
- Hyaline retinal dystrophy
- Degeneration, Stargardt Macular
- Bilateral fundus flavimaculatus of eyes
- STGD
- Sensory retinal dystrophy
Frequently Asked Questions
What is the ICD-10 code for other dystrophies primarily involving the sensory retina?
The ICD-10-CM code for other dystrophies primarily involving the sensory retina is H35.53. The full clinical description is "Other dystrophies primarily involving the sensory retina". H35.53 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H35.53 mean?
ICD-10-CM code H35.53 represents “Other dystrophies primarily involving the sensory retina”. 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 H35.53 a billable code?
Yes, H35.53 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H35.53 in?
H35.53 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What codes cannot be used with H35.53?
H35.53 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 H35.53 map to?
H35.53 maps to 18 SNOMED CT concepts: 12239101000119100, 15628611000119101, 312917007, 35531000119107, 47673003, and 13 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H35.53?
H35.53 is linked to 2 UMLS Concept Unique Identifiers: C0271093, C0154864. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does H35.53 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other dystrophies primarily involving the sensory retina 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 H35.53?
There is no direct ICD-11 mapping available for H35.53 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.