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
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