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Morbid Obesity (CUI C0028756) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0028756

NCI Thesaurus Code: C34858  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

NCIt Definition: An excess of body weight, normally defined as an individual with a body mass index greater than 35 or a body weight greater than one hundred percent of ideal body weight.

MSH Definition: The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2.

Synonyms & Abbreviations: (see Synonym Details)
Adipositas permagna
Morbid Obesities
Morbid obesity (disorder)
Morbid obesity
Obesities, Morbid
Obesities, Severe
Obesity, Morbid [Disease/Finding]
Obesity, Morbid
Obesity, Severe
Severe Obesities
Severe obesity (disorder)
Severe Obesity

External Source Codes: 
NCI Thesaurus Code C34858 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN /surg: consider also BARIATRIC SURGERY MSH
AQL BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CTV3ID X40YQ SNOMEDCT_US
CTV3ID XUt13 SNOMEDCT_US
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DX 19870101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
EFFECTIVE_TIME 20160131 SNOMEDCT_US
FX D007581 MSH
FX D015390 MSH
FX D015391 MSH
FX D015904 MSH
FX D015905 MSH
HN 87 MSH
MDA 19860418 MSH
MESH_DEFINITION The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2. NDFRT
MESH_DUI D009767 NDFRT
MESH_NAME Obesity, Morbid NDFRT
MESH_UI M0015161 NDFRT
MMR 20130708 MSH
MN C18.654.726.500.700 MSH
MN C23.888.144.699.500.500 MSH
MN E01.370.600.115.100.160.120.699.500.500 MSH
MN G07.100.100.160.120.699.500.500 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000002202 NDFRT
PM 87 MSH
RXAUI 3199623 RXNORM
RXAUI 3209570 RXNORM
RXAUI 3209571 RXNORM
RXAUI 5931829 RXNORM
RXCUI 1027600 RXNORM
SMQ_TERM_ADDVERSION 18.1 MDR
SMQ_TERM_ADDVERSION 9.0 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 18.1 MDR
SMQ_TERM_LMVERSION 9.0 MDR
SMQ_TERM_SCOPE 1 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 238136002 NDFRT
SNOMEDID D6-11117 SNOMEDCT_US
SNOMEDID DF-115F1 SNOMEDCT_US
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS E66.8 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS E66.9 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~E66.8 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~E66.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS E66.01 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF EXTREME OBESITY WITH ALVEOLAR HYPOVENTILATION CHOOSE E66.2 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF PROOPIOMELANOCORTIN DEFICIENCY SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447639009 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~2 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~3 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 190966007 | Extreme obesity with alveolar hypoventilation (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 702949005 | Proopiomelanocortin deficiency syndrome (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~OTHERWISE TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~E23.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~E66.01 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~E66.2 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~X40YQ SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUt13 SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~D6-11117 SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~DF-115F1 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
TERMUI T029024 MSH
TERMUI T029025 MSH
TERMUI T840068 MSH
TH NLM (1987) MSH
TH NLM (2014) MSH
TH UNK (19XX) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0028756

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