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What Type of Diabetes?
MODY
What is MODY?
Info on MODY Genetic Subtypes
HNF1A MODY
HNF4A MODY
GCK MODY
HNF1B MODY
KCNJ11 and ABCC8 MODY
Maternally Inherited Diabetes and Deafness (MIDD)
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Next generation sequencing of all known MODY genes
Sanger sequencing of the GCK gene
Sanger sequencing & MLPA of the HNF1B gene
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Sulphonylurea Transfer
GCK Guidelines in Pregnancy
Information on Pregnancy and HNF4A Diabetes
Sulphonylureas & Pregnancy
Find your nearest Monogenic Clinic
Neonatal Diabetes
About Neonatal Diabetes
NDM Genetic Subtypes
Neonatal diabetes caused by mutations in KCNJ11 or ABCC8
6q24 Transient Neonatal Diabetes
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Consent For Diabetes Testing
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Sulphonylurea Transfer In Patients With KCNJ11 And ABCC8 Mutations – TNDM
Sulphonylurea Transfer In Patients With KCNJ11 And ABCC8 Mutations – PNDM
Effects Of Sulphonylurea On The Brain
UK access to Glibenclamide
Specialist multidisciplinary clinics for adults and children with Katp channel-related neonatal diabetes
Rare Types
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Testing Guidelines
Guidelines for Genetic Testing in MODY
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Information for Family Members
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GAD, IA2 & ZnT8 Auto-antibody Testing
Plasma C-peptide Testing
Urine C-peptide Testing
Genetic Tests
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Next Generation Sequencing of all known MODY gene
GCK MODY
HNF1B MODY & Renal Disease
Maternally Inherited Diabetes & Deafness (MIDD)
Non-Invasive Prenatal Testing (NIPT) for monogenic diabetes
Type 1 Diabetes Genetic Risk Score
Interpretation service for MODY gene variants of uncertain significance
Monogenic Autoimmunity
Technical information for Next Generation Sequencing
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Hyperinsulinism
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