loading...| Preferred Name |
Nephroblastoma |
|
| Synonyms |
Wilm's tumor Wilms tumor |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/302849000 |
|
| Active |
1 |
|
| altLabel |
Wilm's tumor Wilms tumour Nephroma Nephroblastoma (disorder) Wilms tumor |
|
| Associated finding of | ||
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005 |
|
| CTV3ID |
Xa9A0 |
|
| cui |
C0027708 |
|
| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20020731 |
|
| Has associated morphology | ||
| Has finding site | ||
| INACTIVATION INDICATOR |
900000000000494007 |
|
| notation |
302849000 |
|
| prefLabel |
Nephroblastoma |
|
| Subset member |
6011000124106~MAPADVICE~IF CHROMOSOME 11P13 DELETION SYNDROME AND IF FEMALE CHOOSE Q52.9 | MAP IS CONTEXT DEPENDENT FOR GENDER 6011000124106~MAPADVICE~IF GLOBAL DEVELOPMENTAL DELAY, LUNG CYSTS, OVERGROWTH, WILMS TUMOR SYNDROME CHOOSE C64.9 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF GLOBAL DEVELOPMENTAL DELAY, LUNG CYSTS, OVERGROWTH, WILMS TUMOR SYNDROME CHOOSE F88 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 4135001 | 11p partial monosomy syndrome (disorder) | 6011000124106~MAPRULE~IFA 1259806004 | Primary nephroblastoma of right kidney | 6011000124106~MAPADVICE~IF POTOCKI-SHAFFER SYNDROME CHOOSE Q93.59 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~F88 6011000124106~MAPTARGET~C64.2 447562003~MAPRULE~TRUE 6011000124106~MAPTARGET~Q93.89 447562003~MAPADVICE~ALWAYS C64 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE 6011000124106~MAPADVICE~IF POTOCKI-SHAFFER SYNDROME CHOOSE Q93.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 1259807008 | Primary nephroblastoma of left kidney | 6011000124106~MAPADVICE~IF WAGR SYNDROME CHOOSE C64.9 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPADVICE~IF 11P PARTIAL MONOSOMY SYNDROME CHOOSE Q93.89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000490003~VALUEID~900000000000494007 6011000124106~MAPTARGET~Q93.59 6011000124106~MAPTARGET~ 6011000124106~MAPRULE~IFA 1082331000119102 | Nephroblastoma of right kidney | 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPRULE~IFA 1082321000119100 | Nephroblastoma of left kidney | 6011000124106~MAPADVICE~IF GLOBAL DEVELOPMENTAL DELAY, LUNG CYSTS, OVERGROWTH, WILMS TUMOR SYNDROME CHOOSE Q87.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPADVICE~IF WAGR SYNDROME CHOOSE Q13.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q52.9 6011000124106~MAPADVICE~ALWAYS C64.9 | CONSIDER LATERALITY SPECIFICATION 6011000124106~MAPADVICE~IF NEPHROBLASTOMA OF LEFT KIDNEY CHOOSE C64.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 782722002 | Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome | 900000000000508004~ACCEPTABILITYID~900000000000549004 6011000124106~MAPADVICE~IF WAGR SYNDROME AND IF FEMALE CHOOSE Q52.9 | MAP IS CONTEXT DEPENDENT FOR GENDER 447562003~MAPTARGET~Q87.8 447562003~MAPGROUP~1 6011000124106~MAPRULE~IFA 702346005 | Chromosome 11p11.2 deletion syndrome (disorder) | 6011000124106~MAPTARGET~F79 6011000124106~MAPADVICE~IF WAGR SYNDROME AND IF MALE CHOOSE Q55.9 | MAP IS CONTEXT DEPENDENT FOR GENDER 447562003~MAPADVICE~IF CHROMOSOME 11P11.2 DELETION SYNDROME CHOOSE Q93.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~CORRELATIONID~447561005 447562003~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF CHROMOSOME 11P11.2 DELETION SYNDROME CHOOSE Q93.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPTARGET~Q55.9 6011000124106~MAPADVICE~IF CHROMOSOME 11P13 DELETION SYNDROME CHOOSE Q13.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q87.3 6011000124106~MAPADVICE~IF CHROMOSOME 11P13 DELETION SYNDROME AND IF MALE CHOOSE Q55.9 | MAP IS CONTEXT DEPENDENT FOR GENDER 447562003~MAPPRIORITY~1 6011000124106~MAPRULE~IFA 715215007 | WAGR syndrome | AND IFA 248153007 | Male (finding) | 6011000124106~MAPRULE~IFA 4135001 | 11p partial monosomy syndrome | 6011000124106~MAPTARGET~Q13.1 447562003~MAPCATEGORYID~447637006 447562003~MAPTARGET~C64 447562003~MAPADVICE~IF 11P PARTIAL MONOSOMY SYNDROME CHOOSE Q87.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q33.0 6011000124106~MAPRULE~IFA 715215007 | Chromosome 11p13 deletion syndrome (disorder) | AND IFA 248153007 | Male (finding) | 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPGROUP~4 6011000124106~MAPRULE~IFA 715215007 | Chromosome 11p13 deletion syndrome (disorder) | 6011000124106~MAPCATEGORYID~447639009 900000000000497000~MAPTARGET~Xa9A0 6011000124106~MAPRULE~IFA 715215007 | WAGR syndrome | AND IFA 248152002 | Female (finding) | 447562003~MAPPRIORITY~3 447562003~MAPRULE~IFA 4135001 | 11p partial monosomy syndrome (disorder) | 447562003~MAPCATEGORYID~447639009 6011000124106~MAPTARGET~Q93.5 6011000124106~MAPPRIORITY~1 6011000124106~MAPPRIORITY~6 6011000124106~MAPADVICE~IF NEPHROBLASTOMA OF RIGHT KIDNEY CHOOSE C64.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 715215007 | WAGR syndrome | 6011000124106~CORRELATIONID~447561005 447562003~MAPTARGET~Q93.5 6011000124106~MAPADVICE~IF GLOBAL DEVELOPMENTAL DELAY, LUNG CYSTS, OVERGROWTH, WILMS TUMOR SYNDROME CHOOSE Q33.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF PRIMARY NEPHROBLASTOMA OF LEFT KIDNEY CHOOSE C64.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 715215007 | Chromosome 11p13 deletion syndrome (disorder) | AND IFA 248152002 | Female (finding) | 447562003~MAPPRIORITY~2 447562003~MAPRULE~IFA 702346005 | Chromosome 11p11.2 deletion syndrome (disorder) | 6011000124106~MAPGROUP~3 6011000124106~MAPRULE~IFA 702346005 | Potocki-Shaffer syndrome | 6011000124106~MAPADVICE~IF CHROMOSOME 11P13 DELETION SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~C64.1 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPADVICE~IF WAGR SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~2 6011000124106~MAPADVICE~IF PRIMARY NEPHROBLASTOMA OF RIGHT KIDNEY CHOOSE C64.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~C64.9 |
|
| tui |
T191 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |