Lissencephaly 2 (norman-roberts type)

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Subtype of: Lissencephaly
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Lissencephaly 2 (Norman-Roberts type)
MONDO_0009760
RELN Unknown
26046367 27000652 17431900 10973257 7682675 35769015
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Lissencephaly 2 (norman-roberts type).
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Sacroiliac arthritis 1 shared geneRELN Related via 1 shared gene including RELN. Sacroiliac joint synovitis 1 shared geneRELN Related via 1 shared gene including RELN. Lissencephaly with cerebellar hypoplasia 1 shared geneRELN Related via 1 shared gene including RELN. Roberts syndrome 1 shared geneRELN Related via 1 shared gene including RELN. Epilepsy with auditory features 1 shared geneRELN Related via 1 shared gene including RELN.