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Summary Literature (1)
MIM:204500 - CEROID LIPOFUSCINOSIS, NEURONAL, 2; CLN2

Xenbase Genes: tpp1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008769 - neuronal ceroid lipofuscinosis 2
MONDO:0015674 - late infantile neuronal ceroid lipofuscinosis
MONDO:0019262 - white matter of myelencephalon

Disease Ontology (DO):
DOID:0110726 - neuronal ceroid lipofuscinosis 2