Lipidoses
Disease ID: disease_node_4786
Connections displayed (default: 10).
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| Dbxref | ICD10CM:E75.6, ICD9CM:272.7, ICD9CM:272.8, MESH:D008064, SNOMEDCT_US_2023_03_01:11455007, SNOMEDCT_US_2023_03_01:154744007, UMLS_CUI:C0023794, UMLS_CUI:C0029591 |
|---|---|
| Subclassof | DOID_3211 |
| Data Source | DOID, MESH |
| Synonyms | Lipoid storage diseas, inborn lipid storage disorder, lipoidosis |
| Mesh Id | D008064 |
| Mesh Label | Lipidoses |
| Mesh Subclassof | D008052 |
| Doid Label | lipid storage disease |
| Doid Description | A lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues. |
| Disease Node Id | disease_node_4786 |
| Doid Id | DOID_9455 |
| Label | Lipidoses |
| Doid Alternate Ids | DOID_10583 |
- Incoming r'ship
SUBCLASS_OFto/from Xanthomatosis(ID:disease_node_8033) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Sphingolipidoses(ID:disease_node_7022) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Siddiqi Syndrome(ID:disease_node_20501) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mucolipidosis(ID:disease_node_20503) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Neuronal Ceroid-Lipofuscinoses(ID:disease_node_5584) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Lysosomal Storage Diseases(ID:disease_node_8717) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lysosomal Acid Lipase Deficiency(ID:disease_node_20502) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Fatty Liver, Alcoholic(ID:disease_node_3194) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Farber Lipogranulomatosis(ID:disease_node_12077) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Fatty Liver(ID:disease_node_3193) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chanarin-Dorfman Syndrome(ID:disease_node_20507) (Disease)