Ciliopathy
Disease ID: disease_node_14682
Connections displayed (default: 10).
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| Subclassof | DOID_225, DOID_0050177 |
|---|---|
| Data Source | DOID |
| Doid Label | ciliopathy |
| Doid Description | A syndrome associated with mutations encoding defective proteins, which result in either abnormal function formation or function of cilia. |
| Disease Node Id | disease_node_14682 |
| Doid Id | DOID_0060340 |
| Disease Has Basis In | SO_0000704 |
| Label | Ciliopathy |
- Incoming r'ship
SUBCLASS_OFto/from Meckel Syndrome(ID:disease_node_14683) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Joubert Syndrome(ID:disease_node_14692) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Ciliary Motility Disorders(ID:disease_node_2113) (Disease)