H35.54
BillableDystrophies primarily w the retinal pigment epithelium
Dystrophies primarily involving the retinal pigment epithelium
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Vitelliform retinal 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
- Cone-rod retinal dystrophy80328002
- Progressive cone-rod dystrophy80328002
- AOFMD - adult-onset foveomacular dystrophy232049001
- AVMD - adult vitelliform macular dystrophy232049001
- Adult vitelliform macular dystrophy232049001
- Adult-onset foveomacular dystrophy232049001
- Adult-onset vitelliform macular dystrophy232049001
- Gass disease232049001
- Pseudo-Best disease232049001
- Pseudo-vitelliform macular dystrophy232049001
- Pattern dystrophy of macula232051002
- Retinal vitelliform deposits247140007
- Macular vitelliform deposits247155003
- Hereditary retinal dystrophy primarily involving retinal pigment epithelium698847000
- Inherited retinal dystrophy primarily involving retinal pigment epithelium698847000
- Amelogenesis imperfecta co-occurrent with cone rod dystrophy707608003
- Jalili syndrome707608003
- Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome719205008
- Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus723408004
- Multifocal pattern dystrophy simulating Stargardt disease723408004
- Multifocal pattern dystrophy simulating fundus flavimaculatus723408004
- Reticular dystrophy of retinal pigment epithelium723502001
- BMD - Best macular dystrophy763387005
- BVMD - Best vitelliform macular dystrophy763387005
- Best disease763387005
- Best vitelliform macular dystrophy763387005
- Early-onset vitelliform macular dystrophy763387005
- Juvenile-onset vitelliform macular dystrophy763387005
- Polymorphic vitelline macular degeneration763387005
- Vitelliform macular dystrophy type 2763387005
- Biallelic RPE65 mutation associated retinal dystrophy764969006
- Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy764969006
- Fundus pulverulentus770437002
- MCRPE - Martinique crinkled retinal pigment epitheliopathy1187639002
- MDPT3 - patterned macular dystrophy 31187639002
- Martinique crinkled retinal pigment epitheliopathy1187639002
- Patterned macular dystrophy 31187639002
- Retinal pigment epithelial dystrophy342581000119102
Frequently Asked Questions
What is the ICD-10 code for dystrophies primarily w the retinal pigment epithelium?
The ICD-10-CM code for dystrophies primarily w the retinal pigment epithelium is H35.54. The full clinical description is "Dystrophies primarily involving the retinal pigment epithelium". H35.54 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H35.54 mean?
ICD-10-CM code H35.54 represents "Dystrophies primarily involving the retinal pigment epithelium". 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 H35.54 a billable code?
Yes, H35.54 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H35.54 in?
H35.54 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What codes cannot be used with H35.54?
H35.54 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 H35.54 map to?
H35.54 maps to 15 SNOMED CT concepts: 232049001, 707608003, 763387005, 764969006, 80328002, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H35.54?
H35.54 is linked to 2 UMLS Concept Unique Identifiers: C0154865, C2880985. 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.