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cone-rod dystrophy 15
Summary
- Synonym
-
- CORD15
- Definition
- A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23.
- Super Class
- cone-rod dystrophy
External Links
- Disease Ontology
- DOID:0111021
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0007994 | Peripheral visual field loss |
| HP:0007703 | Abnormality of retinal pigmentation |
| HP:0001249 | Intellectual disability |
| HP:0007843 | Attenuation of retinal blood vessels |
| HP:0007675 | Progressive night blindness |
| HP:0008046 | Abnormal retinal vascular morphology |
| HP:0001513 | Obesity |
| HP:0007737 | Bone spicule pigmentation of the retina |
| HP:0000551 | Color vision defect |
| 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 |
| 93589 | CACNA2D4 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 |
