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Amyloidosis, familial visceral (CUI C0268389) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0268389

Semantic Type: Congenital Abnormality

Semantic Type: Disease or Syndrome

Synonyms & Abbreviations: (see Synonym Details)
Amyloid nephropathy of Ostertag
Amyloidosis 8
Amyloidosis familial renal
Amyloidosis familial visceral
Amyloidosis systemic nonneuropathic
Amyloidosis VIII
Amyloidosis, familial renal
Amyloidosis, familial visceral
Amyloidosis, Ostertag type
Amyloidosis, systemic nonneuropathic
Familial amyloid nephropathy
Familial renal amyloidosis
Familial visceral amyloidosis, Ostertag type (disorder)
Familial visceral amyloidosis, Ostertag type
German type amyloidosis
Hereditary renal amyloidosis
Ostertag type amyloidosis

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
CHARACTERISTIC_TYPE_ID 900000000000011006 SNOMEDCT_US
CTV3ID X40Pv SNOMEDCT_US
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_CREATED 2015-01-22T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DISEASE_IDENTIFIER_ID 34277 GARD
DISEASE_IDENTIFIER_ID 34278 GARD
DISEASE_IDENTIFIER_ID 34279 GARD
DISEASE_IDENTIFIER_ID 34281 GARD
DISEASE_IDENTIFIER_ID 370 GARD
DISEASE_IDENTIFIER_ID 371 GARD
DISEASE_IDENTIFIER_ID 372 GARD
DISEASE_IDENTIFIER_ID 373 GARD
DISEASE_IDENTIFIER_ID 374 GARD
DISEASE_IDENTIFIER_ID 375 GARD
EFFECTIVE_TIME 20020131 SNOMEDCT_US
FR 1 MSH
GENELOCUS ,1,2,q,1,5, OMIM
GENESYMBOL LYZ OMIM
HAS_GARD_PAGE true GARD
HM D028226 MSH
IDENTIFIER_SOURCE Orp GARD
IDENTIFIER_TYPE_ID 1 GARD
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
MDA 20100825 MSH
MIMTYPE 3 OMIM
MIMTYPEMEANING Phenotype description, molecular basis known. OMIM
MIMTYPEVALUE pound OMIM
MMR 20120824 MSH
MODIFIER_ID 900000000000451002 SNOMEDCT_US
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/8282/amyloidosis-familial-visceral/resources/1 GARD
RN 0 MSH
SC 3 MSH
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS E85.0 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~E85.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS E85.2 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~E85.2 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~X40Pv 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 T745194 MSH
TERMUI T745195 MSH
TERMUI T745196 MSH
TERMUI T745197 MSH
TERMUI T745198 MSH
TERMUI T745199 MSH
TERMUI T824956 MSH
TH OMIM (2013) MSH
TH ORD (2010) 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=C0268389

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