Cortical dysplasia with other brain malformations

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 10
618677C5231458MONDO:0032866
APC2 Causal
22573669 31585108
ClinVar, Disgenet, GWAS catalog, HPO
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 11
620156C5774270MONDO:0859332
KIF26A Causal
36228617 36564622
CTD, ClinVar, Disgenet, HPO
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 12
620316C5830407MONDO:0957217
CAMSAP1 Causal
25363768 28472652 36283405
ClinVar, Disgenet, HPO, Orphanet —
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9
618174C4748540MONDO:0032578
CTNNA2 Causal
24986827 26700408 28250917 28600779 29302074 30013181
ClinVar, Disgenet, GWAS catalog, HPO
All17 Causal4 Unknown14
Related Diseases Diseases that share the most curated genes with Cortical dysplasia with other brain malformations.
5 View disease cluster →
Complex cortical dysplasia with other brain malformations 8 shared genesTUBG1, KIF26A, TUBB2A, KIF5C, TUBB, TUBB3, TUBB2B, KIF2A Related via 8 shared genes including TUBG1, KIF26A, TUBB2A. Tubulinopathy 3 shared genesTUBB2A, TUBB3, TUBB2B Related via 3 shared genes including TUBB2A, TUBB3, TUBB2B. Cortical development malformation 6 shared genesTUBG1, DYNC1H1, KIF5C, TUBB2B, KIF2A, TUBGCP2 Related via 6 shared genes including TUBG1, DYNC1H1, KIF5C. Lissencephaly 8 shared genesTUBG1, CTNNA2, DYNC1H1, TUBB, TUBB3, APC2, TUBB2B, TUBGCP2 Related via 8 shared genes including TUBG1, CTNNA2, DYNC1H1. lissencephaly spectrum disorders 2 shared genesTUBG1, APC2 Related via 2 shared genes including TUBG1, APC2.