Intellectual developmental disorder with short stature, facial anomalies, and speech delay

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Intellectual disability, short stature, facial anomalies, and joint dislocations
MONDO:0011651
FBXL3 Causal — ClinVar, GenCC
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Intellectual developmental disorder with short stature, facial anomalies, and speech delay.
4 View disease cluster →
Short stature 1 shared geneFBXL3 Related via 1 shared gene including FBXL3. Intellectual disability 1 shared geneFBXL3 Related via 1 shared gene including FBXL3. Intellectual developmental disorder 1 shared geneFBXL3 Related via 1 shared gene including FBXL3. Bipolar disorder 1 shared geneFBXL3 Related via 1 shared gene including FBXL3.