Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome

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Subtype of: Short stature
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome
MONDO_0007846
ANKRD11 Unknown
25838844 21782149 2705097 27900361
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome.
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16q24.3 microdeletion syndrome 1 shared geneANKRD11 Related via 1 shared gene including ANKRD11. Kbg 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.