renal hypomagnesemia 6
MONDO:0013480Mondo
Findings
No curated finding names renal hypomagnesemia 6 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset · Childhood onset
HPO, annotations 2026-09-02
Features
5 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.
- HypomagnesemiaHPOHP:0002917
- 4 of 4 reported patients
- Impaired renal tubular reabsorption of magnesiumHPOHP:0033759
- 2 of 2 reported patients
- HeadacheHPOHP:0002315
- 1 of 4 reported patients
- Muscle weaknessHPOHP:0001324
- 1 of 4 reported patients
- VertigoHPOHP:0002321
- 1 of 4 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.
- CNNM2HGNC:103
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
Where it sits
Other names
2 names
Resolves to: renal hypomagnesemia 6
- Also called
- HOMG6renal hypomagnesemia type 6