Statements (15)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
hemoglobin |
| gptkbp:affects |
hemoglobin
|
| gptkbp:cause |
gptkb:methemoglobinemia
|
| gptkbp:causedBy |
mutation in globin genes
|
| gptkbp:diagnosedBy |
blood test
hemoglobin electrophoresis |
| gptkbp:firstDescribed |
1948
|
| https://www.w3.org/2000/01/rdf-schema#label |
hemoglobin M disease
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
609565
|
| gptkbp:symptom |
cyanosis
|
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:Methemoglobinemia
|
| gptkbp:bfsLayer |
6
|