SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome
SETD2 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome.
5 View disease cluster →
SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth 1 shared geneSETD2 Related via 1 shared gene including SETD2. Sotos syndrome 1 shared geneSETD2 Related via 1 shared gene including SETD2. Dandy-walker syndrome 1 shared geneSETD2 Related via 1 shared gene including SETD2. Rhabdomyosarcoma 1 shared geneSETD2 Related via 1 shared gene including SETD2. Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay 1 shared geneSETD2 Related via 1 shared gene including SETD2.