loading...| Preferred Name |
Limited systemic sclerosis |
|
| Synonyms |
Systemic sclerosis, limited Limited scleroderma |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/299276009 |
|
| Active |
1 |
|
| altLabel |
Systemic sclerosis, limited Limited systemic sclerosis (disorder) Limited scleroderma |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XU4VE |
|
| cui |
C0748540 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
299276009 |
|
| prefLabel |
Limited systemic sclerosis |
|
| Subset member |
6011000124106~MAPADVICE~IF CALCINOSIS, RAYNAUD'S PHENOMENON, SCLERODACTYLY, AND TELANGIECTASIA SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 298285004 | Systemic sclerosis with limited cutaneous involvement | 6011000124106~MAPADVICE~IF SYSTEMIC SCLEROSIS WITH LIMITED CUTANEOUS INVOLVEMENT CHOOSE M34.89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 715401008 | Reynolds syndrome | 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 447562003~MAPADVICE~ALWAYS M34.8 6011000124106~MAPTARGET~M34.1 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF REYNOLDS SYNDROME CHOOSE M34.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 298285004 | Systemic sclerosis with limited cutaneous involvement (disorder) | 6011000124106~MAPADVICE~IF CALCINOSIS, RAYNAUD'S PHENOMENON, ESOPHAGEAL DYSMOTILITY, SCLERODACTYLY, AND TELANGIECTASIA SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~ALWAYS M34.9 6011000124106~MAPTARGET~K74.3 6011000124106~MAPADVICE~IF CRST SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 900000000000497000~MAPTARGET~XU4VE 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPADVICE~IF REYNOLDS SYNDROME CHOOSE K74.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPCATEGORYID~447639009 447562003~MAPTARGET~M34.8 6011000124106~MAPRULE~IFA 31848007 | CREST syndrome | 6011000124106~MAPTARGET~M34.89 6011000124106~MAPRULE~IFA 31848007 | Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) | 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPTARGET~M34.9 6011000124106~MAPADVICE~IF CREST SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPRULE~IFA 62382002 | Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder) | 6011000124106~MAPPRIORITY~2 6011000124106~MAPRULE~IFA 62382002 | CRST syndrome | |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |