ketoacidosis due to monocarboxylate transporter-1 deficiency
MONDO:0014490Mondo
Findings
No curated finding names ketoacidosis due to monocarboxylate transporter-1 deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance · Autosomal recessive inheritance
- Onset and course
- Infantile onset · Juvenile onset · Childhood onset
HPO, annotations 2026-09-02
Features
6 features
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.
- KetoacidosisHPOHP:0001993
- 9 of 9 reported patients
- KetonuriaHPOHP:0002919
- 6 of 9 reported patients
- Intellectual disabilityHPOHP:0001249
- 3 of 9 reported patients
- Feeding difficultiesHPOHP:0011968
- Global developmental delayHPOHP:0001263
- Ketotic hypoglycemiaHPOHP:0012734
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.
- SLC16A1HGNC:10922
- Definitive · Ambry Genetics · Autosomal recessive · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · PanelApp Australia · Semidominant · 2025
- Moderate · Ambry Genetics · Semidominant · 2020
- Supportive · Orphanet · Autosomal dominant · 2021