H31.109
BillableChoroidal degeneration, unspecified, unspecified eye
Choroidal degeneration, unspecified, unspecified eye
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)
- angioid streaks of macula (H35.33)
Also Known As / Clinical Terms
SNOMED CT
- Cornea small26098002
- Microcornea26098002
- Hyaline dystrophy of Bruch membrane36524008
- Hyaline dystrophy of Bruch's membrane36524008
- Pseudoinflammatory foveal dystrophy36524008
- Diffuse choriocapillaris atrophy41250005
- Diffuse choroidal sclerosis41250005
- Hereditary choroidal atrophy74469006
- Hereditary choroidal dystrophy74469006
- Chorioretinal atrophy95686007
- Macular choroidal sclerosis247149008
- Chorioretinal degeneration247177004
- Choroidal sclerosis247199007
- Choroidal atrophy247200005
- Choroidal degeneration406446000
- PPA - Peripapillary atrophy420535003
- Peripapillary atrophy420535003
- Choroidal atrophy and alopecia syndrome720850008
- Moloney syndrome720850008
- Regional choroidal atrophy and alopecia720850008
- PPRCA - pigmented paravenous retinochoroidal atrophy723450004
- Pigmented paravenous chorioretinal atrophy723450004
- Pigmented paravenous retinochoroidal atrophy723450004
- Atrophia areata724384008
- Helicoid peripapillary chorioretinal degeneration724384008
- Sveinsson chorioretinal atrophy724384008
- MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome774212003
- MMCAT syndrome774212003
- Microcornea, myopic chorioretinal atrophy, telecanthus syndrome774212003
- Peripheral exudative haemorrhagic chorioretinopathy1285555004
- Peripheral exudative hemorrhagic chorioretinopathy1285555004
Frequently Asked Questions
What is the ICD-10 code for choroidal degeneration, unspecified, unspecified eye?
The ICD-10-CM code for choroidal degeneration, unspecified, unspecified eye is H31.109. The full clinical description is "Choroidal degeneration, unspecified, unspecified eye". H31.109 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H31.109 mean?
ICD-10-CM code H31.109 represents "Choroidal degeneration, unspecified, unspecified eye". 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 H31.109 a billable code?
Yes, H31.109 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H31.109 in?
H31.109 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What SNOMED CT codes does H31.109 map to?
H31.109 maps to 16 SNOMED CT concepts: 724384008, 95686007, 247177004, 247200005, 720850008, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H31.109?
H31.109 is linked to 1 UMLS Concept Unique Identifier: C2880760. 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.