SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Malabsorption of glucose

Synonyms

Malabsorption of glucose (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/267426009

Active

1

altLabel

Malabsorption of glucose (disorder)

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

XE11L

cui

C0271650

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

INACTIVATION INDICATOR

900000000000494007

notation

267426009

prefLabel

Malabsorption of glucose

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

447562003~MAPTARGET~E74.3

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~IF INSULIN RESISTANCE CHOOSE E88.819 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF INSULIN RESISTANCE CHOOSE E88.81 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

900000000000490003~VALUEID~900000000000494007

6011000124106~MAPADVICE~IF INSULIN RESISTANCE - TYPE B CHOOSE E88.81 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

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~MAPPRIORITY~10

6011000124106~MAPTARGET~E88.819

6011000124106~MAPPRIORITY~8

6011000124106~MAPADVICE~ALWAYS E74.39

6011000124106~MAPADVICE~IF MICROCEPHALIC PRIMORDIAL DWARFISM, INSULIN RESISTANCE SYNDROME CHOOSE F89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~E88.818

900000000000508004~ACCEPTABILITYID~900000000000549004

900000000000531004~TARGETCOMPONENT~9414007

6011000124106~MAPRULE~IFA 1220596009 | Microcephalic primordial dwarfism, insulin resistance syndrome |

447562003~MAPGROUP~1

6011000124106~MAPTARGET~Q87.89

447562003~CORRELATIONID~447561005

447562003~MAPADVICE~ALWAYS E74.3

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~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~MAPTARGET~E74.39

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~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

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~MAPRULE~TRUE

6011000124106~MAPGROUP~3

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPRULE~IFA 763325000 | Insulin resistance |

6011000124106~MAPPRIORITY~2

900000000000497000~MAPTARGET~XE11L

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

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/54905006

http://purl.bioontology.org/ontology/SNOMEDCT/190749000

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU003880 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU002023 OMIM CUI
http://purl.bioontology.org/ontology/MDRFRE/10052426 MDRFRE CUI
http://purl.bioontology.org/ontology/RCD/XE11L RCD CUI
http://purl.bioontology.org/ontology/MEDDRA/10008423 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRGER/10052426 MDRGER CUI
http://purl.bioontology.org/ontology/SCTSPA/267426009 SCTSPA CUI
http://purl.bioontology.org/ontology/MDRGER/10024016 MDRGER CUI
http://purl.bioontology.org/ontology/ICD10CM/R73.03 ICD10CM CUI
http://purl.bioontology.org/ontology/MDRFRE/10008423 MDRFRE CUI
http://purl.bioontology.org/ontology/ICPC2P/T99044 ICPC2P CUI
http://purl.bioontology.org/ontology/NDFRT/N0000003651 NDFRT CUI
http://purl.bioontology.org/ontology/MEDDRA/10018429 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10024016 MEDDRA CUI
http://purl.bioontology.org/ontology/ICPC2P/T28003 ICPC2P CUI
http://purl.bioontology.org/ontology/CSP/0862-7400 CRISP CUI
http://purl.bioontology.org/ontology/MDRGER/10018429 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10008423 MDRGER CUI
http://purl.bioontology.org/ontology/MDRFRE/10018429 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10052426 MEDDRA CUI
http://purl.bioontology.org/ontology/MSHFRE/D018149 MSHFRE CUI
http://purl.bioontology.org/ontology/MDRFRE/10024016 MDRFRE CUI
http://purl.bioontology.org/ontology/SNMI/DB-61200 SNMI CUI
http://purl.bioontology.org/ontology/RCD/X40Jh RCD CUI
http://purl.bioontology.org/ontology/SCTSPA/9414007 SCTSPA CUI
http://purl.bioontology.org/ontology/MESH/D018149 MESH CUI
http://purl.bioontology.org/ontology/RCD/XE11L RCD LOOM