Disease #00064 (CLN1 (lipofuscinosis, ceroid, neuronal, type 1 (CLN-1)), OMIM:256730)
| Official abbreviation |
CLN1 |
| Name |
lipofuscinosis, ceroid, neuronal, type 1 (CLN-1) |
| OMIM ID |
256730 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
9 |
| Associated with 1 gene |
PPT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-10-23 09:54:48 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|