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
CNOT1 Causal
31006513 31006510
ClinGen
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. Intellectual developmental disorder 1 shared geneCNOT1 Related via 1 shared gene including CNOT1.