- TypeGroup
- Disease group(s)
- Child entries
- PCBD1-related MODY
- Isolated permanent neonatal diabetes mellitus
- Glutamate dehydrogenase superactivity
- GCK-related disease
- PMM2-CDG
- PGM1-CDG
- Maturity-onset diabetes of the young
- Exercise-induced hyperinsulinism
- MPI-CDG
- Familial hyperinsulinism
- KATP channel-related disease
- HNF4A-related disease
- HNF1A-related disease
- Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- Hepatocyte nuclear factor-1 beta deficiency
- PIK3CA-related overgrowth syndrome
- Uncoupling protein 2 deficiency
- INS-related disease
- Adenosine kinase deficiency
- INSR-related disease
- Insulin promoter factor 1 deficiency
- Mitochondrial pyrimidine nucleotide carrier deficiency
- Phosphatidylinositol 3-kinase regulatory subunit 2 superactivity
- Neurogenic differentiation factor 1 deficiency
- ALG3-CDG
- Krüppel-like factor 11 deficiency
- Carboxyl-ester lipase deficiency
- ALG6-CDG
- PAX4 deficiency
- BLK deficiency
- APPL1 deficiency
- AKT2-related disease
- RFX6 deficiency