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 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
- •angioid streaks of maculaH35.33
Related Codes(3)
Also Known As / Clinical Terms(63)
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
Clinical Terms
- Hereditary choroidal atrophy
- Peripapillary atrophy
- MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome
- Regional choroidal atrophy and alopecia
- Diffuse choriocapillaris atrophy
- Diffuse choroidal sclerosis
- Macular choroidal sclerosis
- Hyaline dystrophy of Bruch's membrane
- PPA - Peripapillary atrophy
- Pigmented paravenous retinochoroidal atrophy
- PPRCA - pigmented paravenous retinochoroidal atrophy
- Choroidal degeneration
- Pseudoinflammatory foveal dystrophy
- Choroidal atrophy and alopecia syndrome
- Cornea small
- Moloney syndrome
- Chorioretinal degeneration
- Peripheral exudative haemorrhagic chorioretinopathy
- Atrophia areata
- Chorioretinal atrophy
- Peripheral exudative hemorrhagic chorioretinopathy
- Microcornea
- Helicoid peripapillary chorioretinal degeneration
- Hereditary choroidal dystrophy
- MMCAT syndrome
- Sveinsson chorioretinal atrophy
- Choroidal sclerosis
- Choroidal atrophy
- Microcornea, myopic chorioretinal atrophy, telecanthus syndrome
- Pigmented paravenous chorioretinal atrophy
- Hyaline dystrophy of Bruch membrane
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.
How does H31.109 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like choroidal degeneration, unspecified, unspecified eye 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 H31.109?
There is no direct ICD-11 mapping available for H31.109 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.