Cowchock syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
COWCHOCK SYNDROME
C0795910MESH:C536450
AIFM1 Unknown
3856385
CTD, Disgenet
RAB33A Unknown — Disgenet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Cowchock syndrome.
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Beta-hydroxyisobutyryl-coa deacylase deficiency 2 shared genesAIFM1, RAB33A Related via 2 shared genes including AIFM1, RAB33A. X-linked hereditary sensory and autonomic neuropathy with deafness 1 shared geneAIFM1 Related via 1 shared gene including AIFM1. Deafness, x-linked 2 shared genesAIFM1, RAB33A Related via 2 shared genes including AIFM1, RAB33A. Charcot-marie-tooth disease, x-linked 1 shared geneAIFM1 Related via 1 shared gene including AIFM1. Spondyloepimetaphyseal dysplasia 2 shared genesAIFM1, RAB33A Related via 2 shared genes including AIFM1, RAB33A.