Ceroid lipofuscinosis, neuronal, 4a (kufs type), autosomal recessive

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Subtype of: Neuronal ceroid lipofuscinosis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Ceroid lipofuscinosis, neuronal, 4A (Kufs type), autosomal recessive
MONDO_0008768
CLN6 Unknown
21549341
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Ceroid lipofuscinosis, neuronal, 4a (kufs type), autosomal recessive.
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Atrophy 1 shared geneCLN6 Related via 1 shared gene including CLN6. Motor skills disorder 1 shared geneCLN6 Related via 1 shared gene including CLN6. Visual disorder 1 shared geneCLN6 Related via 1 shared gene including CLN6. Neuronal ceroid lipofuscinosis 1 shared geneCLN6 Related via 1 shared gene including CLN6. Cystic fibrosis 1 shared geneCLN6 Related via 1 shared gene including CLN6.