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. 2014 Mar 18;2(1):e5. doi: 10.2196/medinform.3172

Table 2.

Clinical Avatars data mapped to the UMLS via MU ontologies.

Clinical Avatars MU source mapping
(direct)
UMLS mapping
(automatic)
Term label
Gender None


F
C0015780 Female

M
C0024554 Male gender
Race OMB standard


African American
C0085756 African American


Native American
C1515945 American Indian or Alaska Native

Asian
C0078988 Asians

White
C0043157 Caucasians

(no data)
C0086409 Hispanic or Latino

Pacific Islander
C1513907 Native Hawaiian or other Pacific Islander

Other/unknown
C1532697 Unknown racial group
Height LOINC:3137-7 C0365282 Body height measured
Weight LOINC:3141-9 C0365286 Body weight measured
BSAa LOINC:3139-3 C0365285 Body surface area measured
INRb LOINC:34714-6 C1369580 INR in blood by coagulation assay value
Smoker



Y SNOMED CT:77176002 C0337664 Smoker

N SNOMED CT:8392000 C0337672 Nonsmoker
DVT c



Y SNOMED CT:128053003 C0149871 Deep venous thrombosis

N SNOMED CT:413076004 C1446197 No past history of venous thrombosis
AMI d







Y SNOMED CT:57054005 C0155626 Acute myocardial infarction

N SNOMED CT:301121007 C0577811 Myocardial perfusion normal
CYP2C9 LNC:46724-1 C1830800 cyp2c9 gene mutations found [identifier] in blood or tissue by molecular genetics method nominal
CYP2C92 LNC:56164-7 C2734139 cyp2c9 gene allele 2 [identifier] in blood by molecular genetics method nominal
CYP2C93 LNC:56165-4 C2734141 cyp2c9 gene allele 3 [identifier] in blood by molecular genetics method nominal
VKORC1 LNC:50722-8 C1978717 vkorc1 gene mutations found [identifier] in blood or tissue by molecular genetics method nominal
VKORC1A LNC:50722-8 C1978717 vkorc1 gene mutations found [identifier] in blood or tissue by molecular genetics method nominal
VKORC1G LNC:50722-8 C1978717 vkorc1 gene mutations found [identifier] in blood or tissue by molecular genetics method nominal
Warfarin RxNorm:11289 C0043031 Warfarin

aBSA=body surface area

bINR=international normalized ratio

cDVT=deep vein thrombosis

dAMI=acute myocardial infarction