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NCIm Version: 201808 (Browser Version 2.9, using LexEVS 6.5.1)
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Thrombomodulin anomalies, familial (CUI C2931365) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C2931365

Semantic Type: Disease or Syndrome

Synonyms & Abbreviations: (see Synonym Details)
Thrombomodulin anomalies, familial

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
FR 1 MSH
HAS_GARD_PAGE true GARD
HM D019851 MSH
IS_RARE true GARD
IS_SPANISH false GARD
MDA 20100825 MSH
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/5195/thrombomodulin-anomalies-familial/resources/1 GARD
RN 0 MSH
SC 3 MSH
TERMUI T740804 MSH
TH ORD (2010) MSH

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C2931365

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