SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Glucose-galactose malabsorption

Synonyms

Glucose-galactose malabsorption (disorder)

Galactose intolerance

ID

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

Active

1

altLabel

Glucose-galactose malabsorption (disorder)

Galactose intolerance

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

C3130

cui

C0016952

C0268186

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

INACTIVATION INDICATOR

900000000000494007

notation

190749000

prefLabel

Glucose-galactose malabsorption

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

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

900000000000497000~MAPTARGET~C3130

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

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

900000000000531004~TARGETCOMPONENT~450849003

tui

T047

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/237972006

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MDRGER/10017605 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10066388 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10017610 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10017604 MDRGER CUI
http://purl.bioontology.org/ontology/MSHFRE/D005693 MSHFRE CUI
http://purl.bioontology.org/ontology/LNC/LP56739-3 LOINC CUI
http://purl.bioontology.org/ontology/MDRFRE/10017605 MDRFRE CUI
http://purl.bioontology.org/ontology/ICD10CM/E74.21 ICD10CM CUI
http://purl.bioontology.org/ontology/LNC/MTHU021572 LOINC CUI
http://purl.bioontology.org/ontology/MDRFRE/10017604 MDRFRE CUI
http://purl.bioontology.org/ontology/OMIM/MTHU012915 OMIM CUI
http://purl.bioontology.org/ontology/MEDDRA/10017610 MEDDRA CUI
http://purl.bioontology.org/ontology/MESH/D005693 MESH CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001303 NDFRT CUI
http://purl.bioontology.org/ontology/MEDDRA/10017605 MEDDRA CUI
http://purl.bioontology.org/ontology/ICD9CM/271.1 ICD9CM CUI
http://purl.bioontology.org/ontology/SNMI/D6-50500 SNMI CUI
http://purl.bioontology.org/ontology/SCTSPA/190745006 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDDRA/10017604 MEDDRA CUI
http://purl.bioontology.org/ontology/SCTSPA/190749000 SCTSPA CUI
http://purl.bioontology.org/ontology/CSP/1849-3608 CRISP CUI
http://purl.bioontology.org/ontology/MDRFRE/10017610 MDRFRE CUI
http://purl.bioontology.org/ontology/RCD/C311. RCD CUI
http://purl.bioontology.org/ontology/OMIM/182380 OMIM CUI
http://purl.bioontology.org/ontology/MESH/C562602 MESH CUI
http://purl.bioontology.org/ontology/ICD10CM/E74.39 ICD10CM CUI
http://purl.bioontology.org/ontology/RCD/C3130 RCD CUI
http://purl.bioontology.org/ontology/MDRFRE/10066388 MDRFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/27943000 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/606824 OMIM CUI
http://purl.bioontology.org/ontology/SCTSPA/190749000 SCTSPA CUI
http://purl.bioontology.org/ontology/SNMI/D6-54320 SNMI CUI
http://purl.bioontology.org/ontology/MEDDRA/10066388 MEDDRA CUI
http://purl.obolibrary.org/obo/MONDO_0011731 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0011731 EFO LOOM
http://nanbyodata.jp/ontology/NANDO_2200909 NANDO LOOM
http://purl.bioontology.org/ontology/MESH/C562602 MESH LOOM
http://purl.bioontology.org/ontology/RCD/C3130 RCD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C562602 RH-MESH LOOM
http://www.orpha.net/ORDO/Orphanet_35710 ORDO LOOM
http://purl.jp/bio/4/id/200906024890422864 IOBC LOOM
http://www.limics.org/hrdo/rdfns#pat_id_10398 HRDO LOOM
http://purl.bioontology.org/ontology/OMIM/606824 OMIM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0268186 OCHV LOOM
http://purl.bioontology.org/ontology/MEDDRA/10066388 MEDDRA LOOM
http://purl.obolibrary.org/obo/MONDO_0011731 DOVES LOOM