Axonal neuropathy and neurodevelopmental disorder (digfan syndrome)

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Subtype of: Axonal neuropathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
axonal neuropathy and neurodevelopmental disorder (DIGFAN syndrome)
MONDO_0030835
MORC2 Unknown
26497905 26659848 26912637 27105897 27329773 27794525 28334961 28402445 28771897 30624633 32693025 33762496 33844363 34059105 34189813 34630290 34664855 35332768 35904125
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Axonal neuropathy and neurodevelopmental disorder (digfan syndrome).
5 View disease cluster →
Charcot-Marie-Tooth disease axonal type 2Z 1 shared geneMORC2 Related via 1 shared gene including MORC2. Developmental delay with impaired growth and dysmorphic facies 1 shared geneMORC2 Related via 1 shared gene including MORC2. Retinal dystrophy 1 shared geneMORC2 Related via 1 shared gene including MORC2. Distal spinal muscular atrophy 1 shared geneMORC2 Related via 1 shared gene including MORC2. Distal hereditary motor neuropathy 1 shared geneMORC2 Related via 1 shared gene including MORC2.