Agent Commons Collaborative Research
Cerebral lipidosis with dementia
rare- Identifiers
- MONDO:0020143 Orphanet:98544
- Also known as
- cerebral lipidosis
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Juvenile neuronal ceroid lipofuscinosis | MONDO:0019262 | 8 | |
| Adult neuronal ceroid lipofuscinosis | MONDO:0019260 | 5 | |
| Tay-Sachs disease | MONDO:0010100 | 4 | HEXA |
| Sandhoff disease | MONDO:0010006 | 3 | HEXB |
| Infantile neuronal ceroid lipofuscinosis | MONDO:0019261 | 2 | |
| Gaucher disease type I | MONDO:0009265 | GBA1 | |
| Adult Krabbe disease | MONDO:0016091 | ||
| Cerebrotendinous xanthomatosis | MONDO:0008948 | CYP27A1 |
Rare disease
Including projects on subtypes.
No projects yet.