Kbg syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
KBG syndrome
MONDO_0007846
ANKRD11 Causal
15378538 15523620 21782149 23184435 23494856 24896178 25413698 25424714 25464108 25529582 25543316 25652421 25838844 26269249 27667800 27900361 28250421 28449295 28566769 28815928 29224748 29565525 30088855 30182498 30877071 31566922 32820523 33262785 33354850 33476899 33653342 33955014 34247373 34547584 35394473 35598261 35682590 35833929 36584991 36628575 37665295
ClinGen, Open Targets —
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.