Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism

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Subtype of: Neurodevelopmental disorder
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism
MONDO_0030999
TTC5 Causal
29302074 32439809
Open Targets
All1 Causal1 Unknown0
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