skip navigation links
National Cancer Institute
Enterprise Vocabulary Services
Box
NCIm Version: 201706 (Browser Version 2.9, using LexEVS 6.5.1)
SearchBox Top
SearchBox Bottom
Weil Disease (CUI C0043102) Suggest changes to this concept
Add to Cart

Terms & Properties

Concept Unique Identifier (CUI): C0043102

Semantic Type: Disease or Syndrome

MSH Definition: A severe form of LEPTOSPIROSIS, usually caused by LEPTOSPIRA INTERROGANS SEROVAR ICTEROHAEMORRHAGIAE and occasionally other serovars. It is transmitted to humans by the rat and is characterized by hemorrhagic and renal symptoms with accompanying JAUNDICE.

Synonyms & Abbreviations: (see Synonym Details)
Disease, Weil's
Disease, Weil
FIEDLER DISEASE
Haemorrhagic leptospiral jaundice
Haemorrhagic leptospirosis with jaundice
Hemorrhagic jaundice
Hemorrhagic leptospiral jaundice
Hemorrhagic leptospiral or spirochetal jaundice
Hemorrhagic leptospirosis with jaundice
Icteric leptospirosis
Icterohemorrhagic fever
Icterohemorrhagic Leptospirosis
Infection due to Leptospira icterohemorrhagiae
Infection due to Leptospira interrogans
JAUNDICE, SPIROCHETAL
LANCEREAUX-MATHIEU-WEIL SPIROCHETOSIS
Leptospiral or spirochetal jaundice (hemorrhagic)
Leptospiral or spirochetal jaundice
Leptospiros icterohem
Leptospirosis icterohaemorrhagica
Leptospirosis icterohemorrhagica (disorder)
Leptospirosis icterohemorrhagica
LEPTOSPIROSIS, ICTEROHEMORRHAGIC
spirochetal jaundice
Weil Disease [Disease/Finding]
WEIL DISEASE
WEIL DIS
Weil's disease (disorder)
Weil's disease
Weils Disease
WEILS DIS

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN if not caused by LEPTOSPIRA INTERROGANS SEROVAR ICTEROHAEMORRHAGIAE, coord IM with specific Leptospira interrogans serovar (IM) or LEPTOSPIRA INTERROGANS (IM) 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 TM UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CHARACTERISTIC_TYPE_ID 900000000000011006 SNOMEDCT_US
CTV3ID XUYTm SNOMEDCT_US
CTV3ID XUYWH SNOMEDCT_US
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DID 0368-3335 CSP
DISEASE_IDENTIFIER_ID 6347 GARD
DISEASE_IDENTIFIER_ID 6350 GARD
DISEASE_IDENTIFIER_ID 6356 GARD
DX 20030101 MSH
EFFECTIVE_TIME 20030731 SNOMEDCT_US
FR 2 MSH
HM D014895 MSH
HN 2003 (1963) MSH
IAN DEFAULT ICD10
ICE Leptospiral or spirochetal jaundice (hemorrhagic); Weil's disease ICD9CM
IDENTIFIER_TYPE_ID 1 GARD
INCLUSION_TERM Leptospirosis due to Leptospira interrogans serovar icterohaemorrhagiae ICD10
IS_ACTIVE true GARD
MDA 19990101 MSH
MDA 20100825 MSH
MESH_DEFINITION A severe form of LEPTOSPIROSIS, usually caused by LEPTOSPIRA INTERROGANS SEROVAR ICTEROHAEMORRHAGIAE and occasionally other serovars. It is transmitted to humans by the rat and is characterized by hemorrhagic and renal symptoms with accompanying JAUNDICE. NDFRT
MESH_DUI D014895 NDFRT
MESH_NAME Weil Disease NDFRT
MESH_UI M0022917 NDFRT
MMR 20090706 MSH
MMR 20091112 MSH
MN C01.252.400.511.739 MSH
MN C01.252.847.511.739 MSH
MODIFIER_ID 900000000000451002 SNOMEDCT_US
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000003157 NDFRT
ORDER_NO 00200 ICD10CM
PM 2003; see WEIL'S DISEASE 1963-2002 MSH
PRIMARY_PATH 10047903$10024234$10004018$10021881$Weil's disease$Leptospira infections$Bacterial infectious disorders$Infections and infestations MDR
PRIMARY_SOC 10021881 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RN 0 MSH
RXAUI 3183588 RXNORM
RXAUI 3188673 RXNORM
RXAUI 3256376 RXNORM
RXAUI 3256377 RXNORM
RXAUI 3256378 RXNORM
RXCUI 1022817 RXNORM
SC 3 MSH
SMQ_TERM_ADDVERSION 8.0 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 8.0 MDR
SMQ_TERM_SCOPE 1 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 398067003 NDFRT
SNOMED_CID 398222003 NDFRT
SNOMEDID DE-1240D SNOMEDCT_US
SNOMEDID DE-1240E SNOMEDCT_US
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS A27.0 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~A27.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS A27.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P53 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF LEPTOSPIRAL HEMORRHAGE AND IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P53 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF LEPTOSPIRAL HEMORRHAGE CHOOSE A27.0 | 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~MAPPRIORITY~4 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 240674005 | Leptospiral hemorrhage (disorder) | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 240674005 | Leptospiral hemorrhage (disorder) | SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~OTHERWISE TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~A27.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~P53 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUYTm SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUYWH SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~DE-1240D SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~DE-1240E SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T043474 MSH
TERMUI T043475 MSH
TERMUI T043476 MSH
TERMUI T043477 MSH
TERMUI T750449 MSH
TERMUI T750450 MSH
TH NLM (1966) MSH
TH ORD (2010) 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=C0043102

Mainbox Bottom