Neurofacioskeletal syndrome with or without renal agenesis

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Subtype of: Renal agenesis
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Neurofacioskeletal syndrome with or without renal agenesis
MONDO_0030966
HS2ST1 Causal
33159882
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Neurofacioskeletal syndrome with or without renal agenesis.
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Multiple congenital anomalies 1 shared geneHS2ST1 Related via 1 shared gene including HS2ST1. Arthrogryposis 1 shared geneHS2ST1 Related via 1 shared gene including HS2ST1. Developmental disorder 1 shared geneHS2ST1 Related via 1 shared gene including HS2ST1. Non-specific syndromic intellectual disability 1 shared geneHS2ST1 Related via 1 shared gene including HS2ST1. Intellectual disability 1 shared geneHS2ST1 Related via 1 shared gene including HS2ST1.