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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02768 | Garg-Mishra progeroid syndrome | ... mandibular hypoplasia, hyperopia, and partial lipodystrophy. It has been reported that mutations in TOMM7 cause this syndrome. TOMM7 encodes a translocase in the outer mitochondrial membrane. The TOMM ... | Congenital malformation | TOMM7 [HSA:54543] [KO:K17771] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |