Lysosomal Storage Diseases
Disease ID: disease_node_8717
Connections displayed (default: 10).
Loading graph...
| Dbxref | MESH:D016464, NCI:C61250, SNOMEDCT_US_2023_03_01:23585005, UMLS_CUI:C0085078 |
|---|---|
| Subclassof | DOID_655 |
| Data Source | DOID, MESH |
| Synonyms | disorder of lysosomal enzyme, inborn lysosomal enzyme disorder, lysosomal storage metabolism disorder |
| Mesh Id | D016464 |
| Mesh Label | Lysosomal Storage Diseases |
| Mesh Subclassof | D008661 |
| Doid Label | lysosomal storage disease |
| Doid Description | An inherited metabolic disorder that involve an abnormal accumulation of substances inside the lysosome resulting from defects in lysosomal function. |
| Disease Node Id | disease_node_8717 |
| Doid Id | DOID_3211 |
| Label | Lysosomal Storage Diseases |
- Incoming r'ship
SUBCLASS_OFto/from Sialic Acid Storage Disease(ID:disease_node_11012) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Schindler Disease(ID:disease_node_20482) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mucopolysaccharidoses(ID:disease_node_5259) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lipidoses(ID:disease_node_4786) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Fucosidosis(ID:disease_node_3340) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Galactosialidosis(ID:disease_node_20486) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Glycogen Storage Disease Type Iib(ID:disease_node_11501) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Cystinosis(ID:disease_node_2358) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Beta-Mannosidosis(ID:disease_node_11225) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Aspartylglucosaminuria(ID:disease_node_11987) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Alpha-Mannosidosis(ID:disease_node_4992) (Disease)