Peho syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
PEHO SYNDROME
C1850055MONDO:00098412605652836MESH:C536317
KIF1A Causal
26486474
Disgenet, GWAS catalog
ZNHIT3 Causal
28335020
CTD, ClinVar, Disgenet, GenCC, HPO, Orphanet —
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Peho syndrome.
5 View disease cluster →
Mayer-rokitansky-kuster-hauser syndrome 1 shared geneZNHIT3 Related via 1 shared gene including ZNHIT3. Sensory neuropathy 1 shared geneKIF1A Related via 1 shared gene including KIF1A. Hereditary sensory and autonomic neuropathy 1 shared geneKIF1A Related via 1 shared gene including KIF1A. syndromic intellectual disability 1 shared geneKIF1A Related via 1 shared gene including KIF1A. Hereditary motor and sensory neuropathies 1 shared geneKIF1A Related via 1 shared gene including KIF1A.