Kbg syndrome

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
KBG syndrome (orofacial clefting, intellectual disability, dental anomalies, dysmorphism)
MONDO_0007846
ANKRD11 Unknown
25838844 21782149 2705097 27900361
Open Targets —
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Kbg syndrome.
5 View disease cluster →
16q24.3 microdeletion syndrome 1 shared geneANKRD11 Related via 1 shared gene including ANKRD11. Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome 1 shared geneANKRD11 Related via 1 shared gene including ANKRD11. Conductive hearing loss 1 shared geneANKRD11 Related via 1 shared gene including ANKRD11. Congenital retrognathism 1 shared geneANKRD11 Related via 1 shared gene including ANKRD11. Astigmatism 1 shared geneANKRD11 Related via 1 shared gene including ANKRD11.