Vitreoretinopathy, Proliferative
Disease ID: disease_node_9745
Connections displayed (default: 10).
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| Dbxref | MESH:D018630, MIM:193235, ORDO:329211, SNOMEDCT_US_2023_03_01:232016005, UMLS_CUI:C0242852 |
|---|---|
| Subclassof | DOID_5679, DOID_9720 |
| Data Source | DOID, MESH |
| Synonyms | ADNIV, Retinitis proliferans, autosomal dominant neovascular inflammatory vitreoretinopathy, proliferative vitreoretinopathy |
| Mesh Id | D018630 |
| Mesh Label | Vitreoretinopathy, Proliferative |
| Mesh Subclassof | D012164 |
| Doid Label | neovascular inflammatory vitreoretinopathy |
| Doid Description | A retinal and vitreous disease characterized by ocular inflammation, vascular dropout, large spots of hyperpigmentation, neovascularization of the peripheral and posterior retina, vitreous hemorrhage, and retinal detachment that has_material_basis_in heterozygous mutation in the CAPN5 gene on chromosome 11q13.5. |
| Has Symptom | SYMP_0000061 |
| Disease Node Id | disease_node_9745 |
| Doid Id | DOID_9719 |
| Label | Vitreoretinopathy, Proliferative |
- Outgoing r'ship
HAS_SYMPTOMto/from Inflammation(ID:disease_node_4305;disease_node_21103) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Vitreous Disease(ID:disease_node_13146) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Retinal Diseases(ID:disease_node_6605) (Disease)