PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0011849|diabetes mellitus |
| Sentences | 4 |
| PubMedID- 23729552 | diabetes mellitus with laron syndrome: case report. |
| PubMedID- 25403779 | Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency. |
| PubMedID- 25005734 | Genetic mutations underlying epimutations have been reported very infrequently in other imprinting disorders, including russell-silver syndrome, transient neonatal diabetes mellitus, and beckwith-wiedemann syndrome associated with kcnq1ot1 (imprinting control region 2) hypomethylation. |
| PubMedID- 24168455 | Eif2ak3 mutations in south indian children with permanent neonatal diabetes mellitus associated with wolcott-rallison syndrome. |
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