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 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)
- hyperornithinemia (E72.4)
- ornithinemia (E72.4)
Also Known As / Clinical Terms
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
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.
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.