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retinitis pigmentosa 86
Summary
- Synonym
-
- RP86
- Definition
- A retinitis pigmentosa characterized by night blindness followed by progressive narrowing of visual fields and decline in visual acuity that has_material_basis_in mutation in the KIAA1549 gene on chromosome 7q34.
- Super Class
- autosomal genetic disease retinitis pigmentosa
External Links
- Disease Ontology
- DOID:0112143
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 330286 | D630045J12Rik | RIKEN cDNA D630045J12 gene |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000613 | Photophobia |
| HP:0000512 | Abnormal electroretinogram |
| HP:0000648 | Optic atrophy |
| HP:0000602 | Ophthalmoplegia |
| HP:0000842 | Hyperinsulinemia |
| HP:0000546 | Retinal degeneration |
| HP:0000618 | Blindness |
| HP:0005978 | Type II diabetes mellitus |
| HP:0007787 | Posterior subcapsular cataract |
| HP:0001347 | Hyperreflexia |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 138050 | HGSNAT | heparan-alpha-glucosaminide N-acetyltransferase |
| 3419 | IDH3A | isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha |
| 3420 | IDH3B | isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta |
| 5158 | PDE6B | phosphodiesterase 6B |
| 55624 | POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
| 762 | CA4 | carbonic anhydrase 4 |
| 79947 | DHDDS | dehydrodolichyl diphosphate synthase subunit |
