Disease #00025 (NCL (Neuronal Ceroid-Lipofuscinoses), OMIM:256370)
Official abbreviation |
NCL |
Name |
Neuronal Ceroid-Lipofuscinoses |
OMIM ID |
256370 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
392 |
Phenotype entries for this disease |
- |
Associated with 11 genes |
CLCN6, CLN3, CLN5, CLN6, CLN8, CTSD, MFSD8, POLG, PPT1, SGSH, TPP1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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