Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary cakut

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Subtype of: Bladder dysfunction
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT
MONDO_0008630
CHRNA3 Unknown
31708116 37161764 38192228 33947782
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary cakut.
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Bladder dysfunction 1 shared geneCHRNA3 Related via 1 shared gene including CHRNA3. Urinary bladder dysfunction 1 shared geneCHRNA3 Related via 1 shared gene including CHRNA3. Autonomic nervous system disease 1 shared geneCHRNA3 Related via 1 shared gene including CHRNA3. Dysautonomia 1 shared geneCHRNA3 Related via 1 shared gene including CHRNA3. Bronchitis 1 shared geneCHRNA3 Related via 1 shared gene including CHRNA3.