Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Neurodevelopmental disorder
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
MONDO_0859179
SUPT16H Causal
31924697 36226587 36255738
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum.
5 View disease cluster →
14q11.2 microduplication syndrome 1 shared geneSUPT16H Related via 1 shared gene including SUPT16H. Abnormality of the corpus callosum 1 shared geneSUPT16H Related via 1 shared gene including SUPT16H. Dextrocardia 1 shared geneSUPT16H Related via 1 shared gene including SUPT16H. Conotruncal cardiac defect 1 shared geneSUPT16H Related via 1 shared gene including SUPT16H. Non-specific syndromic intellectual disability 1 shared geneSUPT16H Related via 1 shared gene including SUPT16H.