hemoglobin M disease (Q55787691)
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human disease
- M hemoglobinopathy
- inherited methemoglobinemia type 2
- generalized reductase deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hemoglobin M disease |
human disease |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference