Autosomal recessive osteopetrosis 8

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Subtype of: Osteopetrosis 8 · Osteoporosis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal recessive osteopetrosis 8
MONDO_0019026
SNX10 Causal
22499339 23123320 23280965
ClinGen, Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Autosomal recessive osteopetrosis 8.
5 View disease cluster →
Liver neoplasms 1 shared geneSNX10 Related via 1 shared gene including SNX10. Osteoporosis 1 shared geneSNX10 Related via 1 shared gene including SNX10. Dental caries 1 shared geneSNX10 Related via 1 shared gene including SNX10. Desbuquois syndrome 1 shared geneSNX10 Related via 1 shared gene including SNX10. Metabolic syndrome 1 shared geneSNX10 Related via 1 shared gene including SNX10.