Disease #00061 (CLN8 (lipofuscinosis, ceroid, neuronal, type 8 (CLN-8)), OMIM:600143)
Official abbreviation |
CLN8 |
Name |
lipofuscinosis, ceroid, neuronal, type 8 (CLN-8) |
OMIM ID |
600143 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
CLN8 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-10-11 12:20:05 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|