type 1 diabetes mellitus 2
Findings
No curated finding names type 1 diabetes mellitus 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited susceptibility or predisposition to developing type 1 diabetes mellitus in which the cause of the disease is a mutation in the INS gene.
Definition from the Mondo Disease Ontology (MONDO:0007454), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Early young adult onset
HPO, annotations 2026-09-02
Features
1 feature
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Type I diabetes mellitusHPOHP:0100651
- 2 of 2 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- INSHGNC:6081
- Strong · Genomics England PanelApp · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
5 names
Resolves to: type 1 diabetes mellitus 2
- Also called
- diabetes mellitus, insulin-dependent, type 2IDDM2INS type 1 diabetes mellitusinsulin-dependent diabetes mellitus 2type 1 diabetes mellitus caused by mutation in INS