H31.20
BillableHereditary choroidal dystrophy, unspecified
Hereditary choroidal dystrophy, unspecified
Coding Notes
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
- •hyperornithinemiaE72.4
- •ornithinemiaE72.4
Related Codes(4)
Also Known As / Clinical Terms(30)
SNOMED CT
- Congenital chorioretinal degeneration24210004
- Hereditary choroidal atrophy74469006
- Hereditary choroidal dystrophy74469006
- Congenital ectopic lens74969002
- Congenital subluxation of lens74969002
- Ectopia lentis74969002
- Choroidal dystrophy312918002
- Autosomal dominant vitreoretinochoroidopathy711162004
- Autosomal dominant vitreoretinochoroidopathy with nanophthalmos711162004
- Vitreoretinochoroidopathy with microcornea, glaucoma and cataract711162004
- Boucher Neuhäuser syndrome715984007
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome715984007
- Ectopia lentis, chorioretinal dystrophy, myopia syndrome722437006
UMLS
Clinical Terms
- Boucher Neuhäuser syndrome
- Autosomal dominant vitreoretinochoroidopathy with nanophthalmos
- Ectopia lentis, chorioretinal dystrophy, myopia syndrome
- Ectopia lentis
- Autosomal dominant vitreoretinochoroidopathy
- Congenital chorioretinal degeneration
- Choroidal dystrophy
- Hereditary choroidal atrophy
- Hereditary choroidal dystrophy (disorder)
- Congenital ectopic lens
- Vitreoretinochoroidopathy with microcornea, glaucoma and cataract
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
- Congenital subluxation of lens
Frequently Asked Questions
What is the ICD-10 code for hereditary choroidal dystrophy, unspecified?
The ICD-10-CM code for hereditary choroidal dystrophy, unspecified is H31.20. The full clinical description is "Hereditary choroidal dystrophy, unspecified". H31.20 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H31.20 mean?
ICD-10-CM code H31.20 represents “Hereditary choroidal dystrophy, unspecified”. 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 H31.20 a billable code?
Yes, H31.20 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H31.20 in?
H31.20 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What SNOMED CT codes does H31.20 map to?
H31.20 maps to 7 SNOMED CT concepts: 711162004, 715984007, 312918002, 24210004, 74969002, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H31.20?
H31.20 is linked to 1 UMLS Concept Unique Identifier: C0154893. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does H31.20 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary choroidal dystrophy, unspecified 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 H31.20?
There is no direct ICD-11 mapping available for H31.20 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.