Glycogen storage disease due to phosphoglycerate kinase 1 deficiency 1187462006
SNOMED CT code
| SNOMED code | 1187462006 |
|---|---|
| name | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency |
| status | active |
| date introduced | 2022-01-31 |
| fully specified name(s) | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Glycogen storage disease due to phosphoglycerate kinase 1 deficiency 1187462006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Glycogen storage disease 29633007 Glycogen storage disease due to phosphoglycerate kinase 1 deficiency 1187462006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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