PedAM
Pediatric Disease Annotations & Medicines
| Disease | dwarfism |
| Phenotype | C0004779|gorlin syndrome |
| Sentences | 1 |
| PubMedID- 22738223 | [88,89] has shown that point mutations in the human orc1, orc4, orc6, cdt1 and cdc6 genes are associated with meier-gorlin syndrome, a form of primordial dwarfism, and several of these mutations were determined to interfere with proper pre-rc formation. |
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