SOX11-related complex neurodevelopmental disorder with or without congenital anomalies

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SOX11-related complex neurodevelopmental disorder with or without congenital anomalies
SOX11 Unknown — ClinGen —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with SOX11-related complex neurodevelopmental disorder with or without congenital anomalies.
5 View disease cluster →
Intellectual developmental disorder microcephaly ocular 1 shared geneSOX11 Related via 1 shared gene including SOX11. Coffin-siris syndrome 1 shared geneSOX11 Related via 1 shared gene including SOX11. Pituitary stalk interruption syndrome 1 shared geneSOX11 Related via 1 shared gene including SOX11. Salivary gland neoplasms 1 shared geneSOX11 Related via 1 shared gene including SOX11. Hypogonadotropic hypogonadism 1 shared geneSOX11 Related via 1 shared gene including SOX11.