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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00271 | Polymicrogyria | Polymicrogyria (PMG) is a malformation of cortical development characterized by an excessive number of small gyri with abnormal lamination. | Congenital malformation |
(BFPP/BFPR) ADGRG1 [HSA:9289] [KO:K08450] (BTOP) FIG4 [HSA:9896] [KO:K22913] (PMGYCHA) PI4KA [HSA:5297] [KO:K00888] (PMGEDSV) COL3A1 [HSA:1281] [KO:K19720] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |