loading...| Preferred Name |
Lipid storage myopathy |
|
| Synonyms |
Lipid storage myopathy (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/240095001 |
|
| Active |
1 |
|
| altLabel |
Lipid storage myopathy (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
X709H |
|
| cui |
C0410214 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has finding site | ||
| notation |
240095001 |
|
| Occurs in | ||
| prefLabel |
Lipid storage myopathy |
|
| Subset member |
447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 725903003 | Autosomal dominant myoglobinuria | 6011000124106~MAPTARGET~G73.7 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPADVICE~IF NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY CHOOSE G73.7 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPTARGET~E75.6 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 447562003~MAPADVICE~ALWAYS E75.6 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~ALWAYS G73.7 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 6011000124106~MAPRULE~IFA 699315005 | Neutral lipid storage disease with myopathy | 900000000000508004~ACCEPTABILITYID~900000000000548007 900000000000497000~MAPTARGET~X709H 6011000124106~MAPADVICE~ALWAYS E75.6 447562003~MAPPRIORITY~1 6011000124106~MAPADVICE~IF NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY CHOOSE E75.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPTARGET~E75.6 447562003~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~IF AUTOSOMAL DOMINANT MYOGLOBINURIA CHOOSE R82.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF GENETIC RECURRENT MYOGLOBINURIA CHOOSE R82.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPTARGET~G72.9 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPRULE~IFA 716721003 | Genetic recurrent myoglobinuria | 6011000124106~MAPRULE~IFA 699315005 | Neutral lipid storage disease with myopathy (disorder) | 6011000124106~MAPTARGET~E75.5 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPADVICE~IF NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY CHOOSE G72.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 716721003 | Genetic recurrent myoglobinuria (disorder) | 6011000124106~MAPPRIORITY~3 6011000124106~MAPPRIORITY~2 6011000124106~MAPTARGET~R82.1 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/10741005 |