Annotation Detail
Information
- Associated Genes
- INS
- Associated Variants
-
INS MUTATION
INS MUTATION - Associated Disease
- DIABETES MELLITUS, PERMANENT NEONATAL
- Source Database
- DisGeNET
- Description
- We report four cases of PNDM.None of the infants or their parents had INS, KCNJ11, or ABCC8 genetic mutations.
- Pubmed
- 25052923
- Section of the abstract supporting the evidence
- CASE PRESENTATION
- Number of the section of the abstract supporting the evidence
- 2
- Number of the sentence supporting the evidence
- 4
- Original source reporting the Gene Disease association
- BeFree,CLINVAR,CTD_human,MGD,ORPHANET,UNIPROT
- DisGENET score for the Gene Disease association
- 0.568414698034489
Drugs