Diseases or functions | p values | Genes | Number of genes |
---|---|---|---|
Neurological disorders | |||
 Growth failure or short stature | 1.58E−07 | Agps, Braf, Cdk13, Dchs1, Efnb2, Fgfr2, Fgfr3, Gja1, Ip6k1, Kdm2a, Kmt2e, Rev3l, Tial1, Trps1, Zbtb20 | 15 |
 Autosomal dominant mental retardation | 1.37E−05 | Cdk13, Chd2, Cic, Kirrel3, Kmt2e, Zbtb20 | 6 |
 Saethre–Chotzen syndrome | 2.07E−05 | Fgfr2, Fgfr3 | 2 |
 Dwarfism | 4.29E−04 | Agps, Fgfr2, Fgfr3, Gja1, Trps1 | 5 |
 Familial congenital anomaly of limb | 4.98E−04 | Fgfr2, Fgfr3, Gja1, Psd3, Trps1 | 5 |
Nervous system development and functions | |||
 Abnormal morphology of neurons | 3.22E−05 | B4galnt1, Braf, Cpeb3, Epha7, Fgfr3, Gja1, Itgb8, Kif5a, Map1a, Wnt4 | 10 |
 Neuritogenesis | 4.35E−05 | Arfgef1, Braf, Cpeb3, Efnb2, Epha7, Fgfr2, Fgfr3, Gja1, Kirrel3, Plxnb1, Rhoq | 11 |
 Proliferation of neuronal cells | 5.14E−05 | Arfgef1, B4galnt1, Braf, Efnb2, Fgfr2, Fgfr3, Gja1, Kdm2a, Rhoq, Spock2 | 10 |
 Branching morphogenesis of nerves | 6.86E−05 | Epha7, Fgfr2 | 2 |