Retinitis Pigmentosa 89
Disease ID: disease_node_15796
Connections displayed (default: 10).
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| Dbxref | MIM:618955 |
|---|---|
| Subclassof | DOID_0050736, DOID_10584 |
| Data Source | DOID |
| Synonyms | RP89 |
| Doid Label | retinitis pigmentosa 89 |
| Doid Description | A retinitis pigmentosa characterized by onset of retinitis pigmentosa in the first decade of life and additional features of ciliopathy that has_material_basis_in heterozygous mutation in the KIF3B gene on chromosome 20q11.21. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15796 |
| Doid Id | DOID_0112146 |
| Label | Retinitis Pigmentosa 89 |
- Outgoing r'ship
SUBCLASS_OFto/from Retinitis Pigmentosa(ID:disease_node_6614) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)