PedAM
Pediatric Disease Annotations & Medicines
| Disease | congenital lymphedema |
| Phenotype | C0025958|microcephaly |
| Sentences | 2 |
| PubMedID- 22284827 | Mutations in kif11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy. |
| PubMedID- 25764055 | Autosomal dominant microcephaly associated with congenital lymphedema and chorioretinopathy due to a novel mutation in kif11. |
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