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Scurvy (CUI C0036474) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0036474

NCI Thesaurus Code: C35010  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

NCIt Definition: Abnormally low concentrations of vitamin C in the blood.

MSH Definition: An acquired blood vessel disorder caused by severe deficiency of vitamin C (ASCORBIC ACID) in the diet leading to defective collagen formation in small blood vessels. Scurvy is characterized by bleeding in any tissue, weakness, ANEMIA, spongy gums, and a brawny induration of the muscles of the calves and legs.

Synonyms & Abbreviations: (see Synonym Details)
Hypoascorbemias
Hypoascorbemia
SCORBUTUS
Scurvies
Scurvy [Disease/Finding]
scurvy
Vitamin C Deficiency
VITAMIN C, INABILITY TO SYNTHESIZE

External Source Codes: 
NCI Thesaurus Code C35010 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
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 900000000000448009 SNOMEDCT_US
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DC 1 MSH
DID 2116-7533 CSP
DISEASE_IDENTIFIER_ID 21761 GARD
DISEASE_IDENTIFIER_ID 21762 GARD
DX 19660101 MSH
FX D001206 MSH
GENELOCUS ,8,p,2,1,.,1, OMIM
GENESYMBOL GULOP OMIM
GENESYMBOL GULO OMIM
HAS_GARD_PAGE true GARD
IDENTIFIER_TYPE_ID 1 GARD
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
MDA 19990101 MSH
MESH_DEFINITION An acquired blood vessel disorder caused by severe deficiency of vitamin C (ASCORBIC ACID) in the diet leading to defective collagen formation in small blood vessels. Scurvy is characterized by bleeding in any tissue, weakness, ANEMIA, spongy gums, and a brawny induration of the muscles of the calves and legs. NDFRT
MESH_DUI D012614 NDFRT
MESH_NAME Scurvy NDFRT
MESH_UI M0019569 NDFRT
MIMTYPE 0 OMIM
MIMTYPEMEANING Other, mainly phenotypes with suspected mendelian basis OMIM
MIMTYPEVALUE none OMIM
MMR 20120703 MSH
MN C14.907.454.800 MSH
MN C15.378.463.515.800 MSH
MN C18.654.521.500.133.115.661 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000002708 NDFRT
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/10406/scurvy/resources/1 GARD
RXAUI 3236947 RXNORM
RXAUI 3236999 RXNORM
RXAUI 3237000 RXNORM
RXAUI 5039486 RXNORM
RXCUI 1025990 RXNORM
SNOMED_CID 76169001 NDFRT
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T037355 MSH
TERMUI T037356 MSH
TERMUI T811893 MSH
TH NLM (1966) MSH
TH OMIM (2013) MSH
TH UNK (19XX) MSH
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=C0036474

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