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| Term | neuronal ceroid lipofuscinosis 9 | ID (Ontology) | DOID:0110733 (Human Disease) |
| Definition | A neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seizures. | ||
| Also Known As | "CLN9" | ||
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autosomal genetic disease |__autosomal recessive disease_____ lipid storage disease | |__neuronal ceroid lipofuscinosis__| neuronal ceroid lipofuscinosis 9 |
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| Is a |
autosomal recessive disease neuronal ceroid lipofuscinosis |
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GARD:6618 ICD10CM:E75.4 MIM:609055 ORDO:228357 |
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