| Glycogen storage disease due to acid maltase deficiency, infantile onset (disorder) | | Glycogen storage disease due to acid maltase deficiency, infantile onset | | Glycogenosis type II, infantile onset
Pompe disease, infantile onset
Glycogen storage disease type II infantile onset
Glycogenosis due to acid maltase deficiency, infantile onset
| | Glycogen storage disease (GSD) due to acid maltase deficiency, classical infantile onset (AMDI), 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 potentially fatal. |
| | Id | 722302009 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | E74.0 | | Rule | TRUE | | Advice | ALWAYS E74.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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