Danon disease 419097006
SNOMED CT code
| SNOMED code | 419097006 |
|---|---|
| name | Danon disease |
| status | active |
| date introduced | 2006-01-31 |
| fully specified name(s) | Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Myocardium structure 74281007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents |
|
| 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 dominant hereditary disease 1162984000 Danon disease 419097006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Lysosomal storage disease 28821000119102 Danon disease 419097006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Glycogen storage disease 29633007 Danon disease 419097006 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Danon disease 419097006 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Myocardial finding 251052000 Myocardial disease 57809008 Cardiomyopathy 85898001 Danon disease 419097006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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