Neurodevelopmental disorder with microcephaly and dysmorphic facies

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Subtype of: Dysmorphic facies · Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodevelopmental disorder with microcephaly and dysmorphic facies
MONDO:0032942
SPOP Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurodevelopmental disorder with microcephaly and dysmorphic facies.
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Neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies 1 shared geneSPOP Related via 1 shared gene including SPOP. Neurodevelopmental disorder, gain of function 1 shared geneSPOP Related via 1 shared gene including SPOP. Nabais sa-de vries syndrome 1 1 shared geneSPOP Related via 1 shared gene including SPOP. Nabais sa-de vries syndrome 2 1 shared geneSPOP Related via 1 shared gene including SPOP. Ductal carcinoma 1 shared geneSPOP Related via 1 shared gene including SPOP.