Holoprosencephaly 12 with or without pancreatic agenesis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Holoprosencephaly 12 with or without pancreatic agenesis
MONDO_0032787
CNOT1 Causal
21679367 31006510 31006513 32553196 35481434
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Holoprosencephaly 12 with or without pancreatic agenesis.
5 View disease cluster →
Vissers-bodmer syndrome 1 shared geneCNOT1 Related via 1 shared gene including CNOT1. Holoprosencephaly 1 shared geneCNOT1 Related via 1 shared gene including CNOT1. Complex neurodevelopmental disorder 1 shared geneCNOT1 Related via 1 shared gene including CNOT1. Non-specific syndromic intellectual disability 1 shared geneCNOT1 Related via 1 shared gene including CNOT1. Global developmental delay 1 shared geneCNOT1 Related via 1 shared gene including CNOT1.