Yemenite deaf-blind hypopigmentation syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME
C1866425
SOX10 Unknown
23982343
Disgenet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Yemenite deaf-blind hypopigmentation syndrome.
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Deaf blind hypopigmentation syndrome 1 shared geneSOX10 Related via 1 shared gene including SOX10. Waardenburg syndrome type 4C 1 shared geneSOX10 Related via 1 shared gene including SOX10. Waardenburg-shah syndrome 1 shared geneSOX10 Related via 1 shared gene including SOX10. Waardenburg syndrome 1 shared geneSOX10 Related via 1 shared gene including SOX10. Growth hormone deficiency 1 shared geneSOX10 Related via 1 shared gene including SOX10.