Congenital microcephaly

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL MICROCEPHALY - SEVERE ENCEPHALOPATHY - PROGRESSIVE CEREBRAL ATROPHY SYNDROME
MONDO:0014258
ASNS Causal
32481472 32255274 31720226 31123592 30978478 30057589 29375865 29279279 28776279 27743885 27522229 27469131 27422383 27268761 25663424 25227173 24139043
ClinGen, ClinVar, GWAS catalog
All31 Causal1 Unknown31
Related Diseases Diseases that share the most curated genes with Congenital microcephaly.
5 View disease cluster →
Primary microcephaly 10 shared genesASPM, CDK5RAP2, MCPH1, CIT, WDR62, CEP152, CPAP, KNL1, PHC1, STIL Related via 10 shared genes including ASPM, CDK5RAP2, MCPH1. Microcephaly 15 shared genesFOXG1, CASK, ASPM, CDK5RAP2, PNKP, MCPH1, CIT, WDR62, CEP152, CPAP, KNL1, PHC1 +3 more Related via 15 shared genes including FOXG1, CASK, ASPM. autosomal recessive primary microcephaly 3 shared genesASPM, CDK5RAP2, STIL Related via 3 shared genes including ASPM, CDK5RAP2, STIL. Seckel syndrome 4 shared genesCDK5RAP2, CEP152, CPAP, RNF17 Related via 4 shared genes including CDK5RAP2, CEP152, CPAP. Lissencephaly 6 shared genesFOXG1, CASK, ASPM, CPAP, TUBA3E, MZT2B Related via 6 shared genes including FOXG1, CASK, ASPM.