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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02663 | Braddock-Carey syndrome | ... has been identified as de novo microdeletions at 21q22.11. It has also been reported that mutations in KIF15 (chromosome 3p21) cause BRDCS. KIF15 is a member of the kinesin superfamily, microtubule-based ... | Congenital malformation | (BRDCS2) KIF15 [HSA:56992] [KO:K10400] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |