Disease & disorder
glycogen storage disease due to acid maltase deficiency, infantile onset
MONDO:0017694
Glycogen storage disease due to acid maltase deficiency, infantile onset is the most severe form of glycogen storage disease due to acid maltase deficiency, characterized by cardiomegaly with respiratory distress, muscle weakness and feeding difficulties. It is often fatal.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to glycogen storage disease due to acid maltase deficiency, infantile onset. Results are keyword matches, not yet verified disease-to-outbreak relationships.
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Background context
glycogen storage disease due to acid maltase deficiency, infantile onset
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.