neuronal ceroid lipofuscinosis 3
condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments
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neuronal ceroid lipofuscinosis 3
Summary
neuronal ceroid lipofuscinosis 3 is a class of disease[1].
Key Facts
- neuronal ceroid lipofuscinosis 3's instance of is recorded as class of disease[2].
- neuronal ceroid lipofuscinosis 3 is a type of neuronal ceroid lipofuscinosis[3].
- neuronal ceroid lipofuscinosis 3 is a type of juvenile neuronal ceroid lipofuscinosis[4].
- neuronal ceroid lipofuscinosis 3 is a type of genetic disease[5].
- neuronal ceroid lipofuscinosis 3's NCI Thesaurus ID is recorded as C61258[6].
- neuronal ceroid lipofuscinosis 3's genetic association is recorded as CLN3[7].
- neuronal ceroid lipofuscinosis 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110731[8].
- neuronal ceroid lipofuscinosis 3's exact match is recorded as http://identifiers.org/doid/DOID:0110731[9].
- neuronal ceroid lipofuscinosis 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_228346[10].
- neuronal ceroid lipofuscinosis 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79264[11].
- neuronal ceroid lipofuscinosis 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].