loading...| Preferred Name | Secondary Raynaud's phenomenon | |
| Synonyms |
Secondary Raynaud phenomenon Secondary Raynaud's phenomenon (finding) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/356198000 |
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| Active |
1 |
|
| altLabel |
Secondary Raynaud phenomenon Secondary Raynaud's phenomenon (finding) |
|
| CASE SIGNIFICANCE ID |
900000000000020002 |
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| Cause of |
http://purl.bioontology.org/ontology/SNOMEDCT/286311000119104 |
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| CTV3ID |
XU66h |
|
| cui |
C1282916 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
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| Has finding site | ||
| notation |
356198000 |
|
| prefLabel |
Secondary Raynaud's phenomenon |
|
| 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 447562003~MAPTARGET~I73.0 447562003~MAPTARGET~M34.1 6011000124106~MAPADVICE~IF RAYNAUD PHENOMENON DUE TO AUTOIMMUNE DISEASE CHOOSE I73.00 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 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~MAPRULE~IFA 62382002 | Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder) | 6011000124106~MAPTARGET~M34.1 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 447562003~MAPADVICE~IF CALCINOSIS, RAYNAUD'S PHENOMENON, SCLERODACTYLY, AND TELANGIECTASIA SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~CORRELATIONID~447561005 447562003~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~IF RAYNAUD PHENOMENON DUE TO AUTOIMMUNE DISEASE CHOOSE M35.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000509007~ACCEPTABILITYID~900000000000548007 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~IF CRST SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447639009 900000000000497000~MAPTARGET~XU66h 6011000124106~MAPRULE~IFA 31848007 | CREST syndrome | 447562003~MAPADVICE~ALWAYS I73.0 | POSSIBLE REQUIREMENT FOR CAUSATIVE AGENT CODE 447562003~MAPPRIORITY~3 6011000124106~MAPTARGET~I73.00 6011000124106~MAPRULE~IFA 31848007 | Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) | 447562003~MAPCATEGORYID~447639009 447562003~MAPADVICE~IF A CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPTARGET~M35.9 447562003~MAPRULE~IFA 31848007 | Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) | 447562003~MAPPRIORITY~2 6011000124106~MAPADVICE~IF CREST SYNDROME CHOOSE M34.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~3 6011000124106~MAPRULE~IFA 1208849004 | Raynaud phenomenon due to autoimmune disease | 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 | 6011000124106~MAPADVICE~ALWAYS I73.00 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |