hemoglobin M disease
MONDO:0018023Mondo
Findings
No curated finding names hemoglobin M disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Genes
3 genes
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.
- HBBHGNC:4827
- Definitive · ClinGen · Autosomal dominant · 2024
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2018
- Supportive · Orphanet · Autosomal dominant · 2021
- HBA1; HBA2HGNC:4824
- Supportive · Orphanet · Autosomal dominant · 2021
- HBA1; HBA2HGNC:4823
- Supportive · Orphanet · Autosomal dominant · 2021
Where it sits
- A kind of
Other names
2 names
Resolves to: hemoglobin M disease
- Also called
- M hemoglobinopathymethemoglobinemia, beta type