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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00267 | Holoprosencephaly | Holoprosencephaly (HPE) is characterized by incomplete separation of forebrain and facial components into left and right sides. | Congenital malformation |
(HPE2) SIX3 [HSA:6496] [KO:K19473] (HPE3) SHH [HSA:6469] [KO:K11988] (HPE4) TGIF1 [HSA:7050] [KO:K19383] (HPE5) ZIC2 [HSA:7546] [KO:K06235] (HPE7) PTCH1 [HSA:5727] [KO:K06225] (HPE9) GLI2 [HSA:2736] [KO:K16798] (HPE11) CDON [HSA:50937] [KO:K20033] (HPE12) CNOT1 [HSA:23019] [KO:K12604] (HPE13) STAG2 [HSA:10735] [KO:K06671] (HPE14) PLCH1 [HSA:23007] [KO:K19006] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |