Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities

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
INTS11-related neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
MONDO_0957386
INTS11 Unknown
37980560 37054711
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities.
5 View disease cluster →
Non-specific syndromic intellectual disability 1 shared geneINTS11 Related via 1 shared gene including INTS11. Inflammatory bowel disease 1 shared geneINTS11 Related via 1 shared gene including INTS11. Ulcerative colitis 1 shared geneINTS11 Related via 1 shared gene including INTS11. Crohn disease 1 shared geneINTS11 Related via 1 shared gene including INTS11. Neurodevelopmental disorder 1 shared geneINTS11 Related via 1 shared gene including INTS11.