Punctate inner choroidopathy
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare ophthalmic disorder characterized by typically bilateral, asymmetric, yellowish, punctate chorioretinal lesions of the posterior pole forming a linear branching pattern and progressing to atrophic scars. Subretinal neovascular membranes occur in many cases. Vitritis is always absent. Patients may present with blurred vision, scotoma, floaters, photopsia, and metamorphopsia. Choroidal neovascular membrane formation and subretinal fibrosis are the major causes of visual loss. The condition predominantly occurs in young myopic females.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Punctate inner choroidopathy | |
| fr | Choroïdopathie interne ponctuée | |
| de | Punktförmige innere Choroidopathie | PIC |
| es | Coroidopatía punteada interna | Coroidopatía punctata interna |
| it | Coroidopatia puntata interna | |
| nl | Puntvormige interne choroïdopathie | |
| pt | Coroidopatia interna punctiforme | Coroidopatia interna punctata |
| pl | Punktowa choroidopatia wewnętrzna | |
| cs | Punkční vnitřní choroidopatie | |
| uk | Точкова внутрішня хоріодопатія | |
| zh | 点状内脉络膜病变 | |
| tr | Noktalı iç koroidopatisi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H31.0 | NTBT | attributed | not yet validated |
| ICD-11 | 9B65.0 | NTBT | index | validated |
| MONDO | 0035584 | E | validated | |
| UMLS | C0730321 | E | validated | |
| GARD | 7503 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:90061Non-infectious posterior uveitis
rare ophthalmic disorders - ORPHA:716195Rare inflammatory choroidal disorder
rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/580951
- This record as JSON: /data/d/580951.json