loading...| Preferred Name |
Insulin resistance |
|
| Synonyms |
Insulin resistance (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/763325000 |
|
| Active |
1 |
|
| altLabel |
Insulin resistance (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XV1se |
|
| cui |
C0021655 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20180731 |
|
| Has finding site | ||
| notation |
763325000 |
|
| prefLabel |
Insulin resistance |
|
| Subset member |
6011000124106~MAPTARGET~E11.9 6011000124106~MAPTARGET~E34.328 6011000124106~MAPTARGET~E88.81 447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 237651005 | Insulin resistance - type A | 6011000124106~MAPADVICE~IF LEPRECHAUNISM SYNDROME CHOOSE E34.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E88.811 6011000124106~MAPTARGET~E13.69 6011000124106~MAPADVICE~IF INSULIN RESISTANCE - TYPE A CHOOSE E88.81 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF MICROCEPHALIC PRIMORDIAL DWARFISM, INSULIN RESISTANCE SYNDROME CHOOSE Q02 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~ 6011000124106~MAPTARGET~P05.9 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPRULE~IFA 1197747005 | Autosomal semi-dominant severe lipodystrophic laminopathy | 6011000124106~MAPTARGET~E88.819 6011000124106~MAPPRIORITY~8 6011000124106~MAPADVICE~IF MICROCEPHALIC PRIMORDIAL DWARFISM, INSULIN RESISTANCE SYNDROME CHOOSE F89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E88.818 447562003~MAPTARGET~E74.8 6011000124106~MAPRULE~IFA 1220596009 | Microcephalic primordial dwarfism, insulin resistance syndrome | 447562003~MAPGROUP~1 6011000124106~MAPTARGET~Q87.89 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF INSULIN RESISTANCE - TYPE A CHOOSE E88.811 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF MICROCEPHALIC PRIMORDIAL DWARFISM, INSULIN RESISTANCE SYNDROME CHOOSE E88.819 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPTARGET~E88.1 6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, SHORT STATURE, EARLY ADULT-ONSET DIABETES SYNDROME CHOOSE E34.328 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPPRIORITY~1 6011000124106~MAPRULE~IFA 1197592001 | Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome | 447562003~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~IF INSULIN RESISTANCE - TYPE A CHOOSE E13.69 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPGROUP~4 6011000124106~MAPADVICE~ALWAYS E88.819 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 6011000124106~MAPADVICE~IF INSULIN RESISTANCE - TYPE B CHOOSE E88.818 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~9 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, SHORT STATURE, EARLY ADULT-ONSET DIABETES SYNDROME CHOOSE E11.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~ALWAYS E88.81 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 447562003~MAPADVICE~ALWAYS E74.8 6011000124106~MAPADVICE~IF AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY CHOOSE E88.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF MICROCEPHALIC PRIMORDIAL DWARFISM, INSULIN RESISTANCE SYNDROME CHOOSE E88.81 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~1 6011000124106~MAPTARGET~F89 6011000124106~MAPRULE~IFA 63702009 | Alstrom syndrome | 6011000124106~MAPTARGET~E34.8 6011000124106~MAPPRIORITY~6 900000000000497000~MAPTARGET~XV1se 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~IFA 237652003 | Insulin resistance - type B | 6011000124106~MAPADVICE~IF MICROCEPHALIC PRIMORDIAL DWARFISM, INSULIN RESISTANCE SYNDROME CHOOSE E34.328 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF ALSTROM SYNDROME CHOOSE Q87.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 111307005 | Leprechaunism syndrome | 6011000124106~MAPRULE~IFA 783616005 | Perilipin 1 related familial partial lipodystrophy | 6011000124106~MAPTARGET~Q02 6011000124106~MAPGROUP~3 6011000124106~MAPPRIORITY~3 6011000124106~MAPPRIORITY~2 6011000124106~MAPADVICE~IF PERILIPIN 1 RELATED FAMILIAL PARTIAL LIPODYSTROPHY CHOOSE E88.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, SHORT STATURE, EARLY ADULT-ONSET DIABETES SYNDROME CHOOSE P05.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT |
|
| tui |
T046 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/362969004 |