Neurodevelopmental delay, congenital heart defects, and distinct facial dysmorphism

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Subtype of: Neurodevelopmental delay
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neurodevelopmental delay, congenital heart defects, and distinct facial dysmorphism
MONDO_0032672
TMEM94 Unknown
30526868
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Neurodevelopmental delay, congenital heart defects, and distinct facial dysmorphism.
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Intellectual developmental disorder dysmorphic cardiac 1 shared geneTMEM94 Related via 1 shared gene including TMEM94. Congenital neurologic anomalies 1 shared geneTMEM94 Related via 1 shared gene including TMEM94. Post-traumatic stress disorder 1 shared geneTMEM94 Related via 1 shared gene including TMEM94. Dementia 1 shared geneTMEM94 Related via 1 shared gene including TMEM94. Alzheimer disease 1 shared geneTMEM94 Related via 1 shared gene including TMEM94.