Logica COVID-19 FHIR Profile Library IG
0.13.1 - ci-build
Logica COVID-19 FHIR Profile Library IG
0.13.1 - ci-build
Logica COVID-19 FHIR Profile Library IG - Local Development build (v0.13.1). See the Directory of published versions
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<ValueSet xmlns="http://hl7.org/fhir">
<id value="covid19-underlying-metabolic-condition-value-set"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><ul><li>Include these codes as defined in <a href="http://www.snomed.org/"><code>http://snomed.info/sct</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=267454002">267454002</a></td><td>Acatalasemia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238069004">238069004</a></td><td>Acyl-coenzyme A oxidase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=363732003">363732003</a></td><td>Addison's disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=386584007">386584007</a></td><td>Adrenal cortical hypofunction (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=237735008">237735008</a></td><td>Adrenal Cushing's syndrome (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=65389002">65389002</a></td><td>Adrenoleukodystrophy (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=700463002">700463002</a></td><td>Alpha-methylacyl-CoA racemase deficiency disorder (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=54954004">54954004</a></td><td>Aspartylglucosaminuria (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238068007">238068007</a></td><td>Bifunctional peroxisomal enzyme deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=128289001">128289001</a></td><td>Chronic metabolic disorder (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=7573000">7573000</a></td><td>Classical phenylketonuria (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=35691006">35691006</a></td><td>Combined deficiency of sialidase AND beta galactosidase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=237751000">237751000</a></td><td>Congenital adrenal hyperplasia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=419097006">419097006</a></td><td>Danon disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=124302001">124302001</a></td><td>Deficiency of galactokinase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=124437004">124437004</a></td><td>Deficiency of glucose-6-phosphatase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=124335006">124335006</a></td><td>Deficiency of phosphoglycerate kinase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=124675005">124675005</a></td><td>Deficiency of phosphoglycerate mutase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=387817006">387817006</a></td><td>Deficiency of phosphorylase b kinase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=124329006">124329006</a></td><td>Deficiency of phosphorylase kinase (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=46635009">46635009</a></td><td>Diabetes mellitus type 1 (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=44054006">44054006</a></td><td>Diabetes mellitus type 2 (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=73211009">73211009</a></td><td>Diabetes mellitus (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=45744005">45744005</a></td><td>Disorder of mineral metabolism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238059005">238059005</a></td><td>Disorder of peroxisomal function (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238006008">238006008</a></td><td>Disorder of purine and pyrimidine metabolism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=30171000">30171000</a></td><td>Disorder of adrenal gland (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=73132005">73132005</a></td><td>Disorder of parathyroid gland (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=399244003">399244003</a></td><td>Disorder of pituitary gland (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=190680002">190680002</a></td><td>Disorders of amino acid transport and metabolism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=16652001">16652001</a></td><td>Fabry's disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=79935000">79935000</a></td><td>Farber's lipogranulomatosis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=717276003">717276003</a></td><td>Folinic acid responsive seizure syndrome (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=20052008">20052008</a></td><td>Fructose-1,6-bisphosphate aldolase B deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=28183005">28183005</a></td><td>Fructose-biphosphatase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=190745006">190745006</a></td><td>Galactosemia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=192782005">192782005</a></td><td>Galactosylceramide beta-galactosidase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=190794006">190794006</a></td><td>Glucosylceramide beta-glucosidase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=235908005">235908005</a></td><td>Glycogen storage disease type IX (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=41527003">41527003</a></td><td>Glycogen storage disease type VIII (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=37666005">37666005</a></td><td>Glycogen storage disease type X (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=717821004">717821004</a></td><td>Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=7265005">7265005</a></td><td>Glycogen storage disease, type I (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=274864009">274864009</a></td><td>Glycogen storage disease, type II (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=66937008">66937008</a></td><td>Glycogen storage disease, type III (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=11179002">11179002</a></td><td>Glycogen storage disease, type IV (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=55912009">55912009</a></td><td>Glycogen storage disease, type V (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=29291001">29291001</a></td><td>Glycogen storage disease, type VI (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=89597008">89597008</a></td><td>Glycogen storage disease, type VII (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=237964009">237964009</a></td><td>Glycogen synthase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=61598006">61598006</a></td><td>Glycogenosis with glucoaminophosphaturia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238025006">238025006</a></td><td>GM1 gangliosidosis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=353295004">353295004</a></td><td>Graves' disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=21983002">21983002</a></td><td>Hashimoto thyroiditis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=111578003">111578003</a></td><td>Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=66999008">66999008</a></td><td>Hyperparathyroidism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=10649000">10649000</a></td><td>Hyperpituitarism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=34486009">34486009</a></td><td>Hyperthyroidism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=36976004">36976004</a></td><td>Hypoparathyroidism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=74728003">74728003</a></td><td>Hypopituitarism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=40930008">40930008</a></td><td>Hypothyroidism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=70199000">70199000</a></td><td>I-cell disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=86095007">86095007</a></td><td>Inborn error of metabolism (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238062008">238062008</a></td><td>Infantile Refsum's disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=18756002">18756002</a></td><td>Juvenile GM1 gangliosidosis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=65524005">65524005</a></td><td>Mannosidosis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=27718001">27718001</a></td><td>Maple syrup urine disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=69463008">69463008</a></td><td>Maroteaux-Lamy syndrome (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=237602007">237602007</a></td><td>Metabolic syndrome X (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=396338004">396338004</a></td><td>Metachromatic leucodystrophy (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=725296006">725296006</a></td><td>Mucolipidosis type IV (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=75610003">75610003</a></td><td>Mucopolysaccharidosis type I (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=65327002">65327002</a></td><td>Mucopolysaccharidosis type I-H (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=26745009">26745009</a></td><td>Mucopolysaccharidosis type I-H/S (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=70737009">70737009</a></td><td>Mucopolysaccharidosis type II (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=73123008">73123008</a></td><td>Mucopolysaccharidosis type I-S (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=43916004">43916004</a></td><td>Mucopolysaccharidosis type VII (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=378007">378007</a></td><td>Morquio syndrome (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=238061001">238061001</a></td><td>Neonatal adrenoleucodystrophy (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=783717008">783717008</a></td><td>Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=5335002">5335002</a></td><td>Phosphoenolpyruvate carboxykinase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=25362006">25362006</a></td><td>Phytanic acid storage disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=65520001">65520001</a></td><td>Primary hyperoxaluria, type I (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=65764006">65764006</a></td><td>Pseudo-Hurler polydystrophy (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=734434007">734434007</a></td><td>Pyridoxine-dependent epilepsy (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=46683007">46683007</a></td><td>Pyruvate dehydrogenase complex deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=23849003">23849003</a></td><td>Sandhoff disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=88393000">88393000</a></td><td>Sanfilippo syndrome (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=38795005">38795005</a></td><td>Sialidosis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=58459009">58459009</a></td><td>Sphingomyelin/cholesterol lipidosis (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=34420000">34420000</a></td><td>Storage disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=367368009">367368009</a></td><td>Sulfite oxidase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=111385000">111385000</a></td><td>Tay-Sachs disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=264580006">264580006</a></td><td>Thyroid dysfunction (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=8849004">8849004</a></td><td>Uridine diphosphate glucose-4-epimerase deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=88469006">88469006</a></td><td>Zellweger syndrome (disorder)</td></tr></table></li></ul></div>
</text>
<url
value="http://fhir.logicahealth.org/covid19/ValueSet/covid19-underlying-metabolic-condition-value-set"/>
<version value="0.13.1"/>
<name value="COVID19UnderlyingMetabolicConditionVS"/>
<title value="COVID-19 metabolic underlying condition reference set"/>
<status value="active"/>
<date value="2021-08-09T20:08:14+00:00"/>
<publisher value="Logica"/>
<contact>
<name value="Logica"/>
<telecom>
<system value="url"/>
<value value="https://www.logicahealth.org/"/>
</telecom>
</contact>
<description
value="A set of codes that describe underlying metabolic conditions for COVID19"/>
<compose>
<include>
<system value="http://snomed.info/sct"/>
<concept>
<code value="267454002"/>
<display value="Acatalasemia (disorder)"/>
</concept>
<concept>
<code value="238069004"/>
<display value="Acyl-coenzyme A oxidase deficiency (disorder)"/>
</concept>
<concept>
<code value="363732003"/>
<display value="Addison's disease (disorder)"/>
</concept>
<concept>
<code value="386584007"/>
<display value="Adrenal cortical hypofunction (disorder)"/>
</concept>
<concept>
<code value="237735008"/>
<display value="Adrenal Cushing's syndrome (disorder)"/>
</concept>
<concept>
<code value="65389002"/>
<display value="Adrenoleukodystrophy (disorder)"/>
</concept>
<concept>
<code value="700463002"/>
<display
value="Alpha-methylacyl-CoA racemase deficiency disorder (disorder)"/>
</concept>
<concept>
<code value="54954004"/>
<display value="Aspartylglucosaminuria (disorder)"/>
</concept>
<concept>
<code value="238068007"/>
<display value="Bifunctional peroxisomal enzyme deficiency (disorder)"/>
</concept>
<concept>
<code value="128289001"/>
<display value="Chronic metabolic disorder (disorder)"/>
</concept>
<concept>
<code value="7573000"/>
<display value="Classical phenylketonuria (disorder)"/>
</concept>
<concept>
<code value="35691006"/>
<display
value="Combined deficiency of sialidase AND beta galactosidase (disorder)"/>
</concept>
<concept>
<code value="237751000"/>
<display value="Congenital adrenal hyperplasia (disorder)"/>
</concept>
<concept>
<code value="419097006"/>
<display value="Danon disease (disorder)"/>
</concept>
<concept>
<code value="124302001"/>
<display value="Deficiency of galactokinase (disorder)"/>
</concept>
<concept>
<code value="124437004"/>
<display value="Deficiency of glucose-6-phosphatase (disorder)"/>
</concept>
<concept>
<code value="124335006"/>
<display value="Deficiency of phosphoglycerate kinase (disorder)"/>
</concept>
<concept>
<code value="124675005"/>
<display value="Deficiency of phosphoglycerate mutase (disorder)"/>
</concept>
<concept>
<code value="387817006"/>
<display value="Deficiency of phosphorylase b kinase (disorder)"/>
</concept>
<concept>
<code value="124329006"/>
<display value="Deficiency of phosphorylase kinase (disorder)"/>
</concept>
<concept>
<code value="46635009"/>
<display value="Diabetes mellitus type 1 (disorder)"/>
</concept>
<concept>
<code value="44054006"/>
<display value="Diabetes mellitus type 2 (disorder)"/>
</concept>
<concept>
<code value="73211009"/>
<display value="Diabetes mellitus (disorder)"/>
</concept>
<concept>
<code value="45744005"/>
<display value="Disorder of mineral metabolism (disorder)"/>
</concept>
<concept>
<code value="238059005"/>
<display value="Disorder of peroxisomal function (disorder)"/>
</concept>
<concept>
<code value="238006008"/>
<display value="Disorder of purine and pyrimidine metabolism (disorder)"/>
</concept>
<concept>
<code value="30171000"/>
<display value="Disorder of adrenal gland (disorder)"/>
</concept>
<concept>
<code value="73132005"/>
<display value="Disorder of parathyroid gland (disorder)"/>
</concept>
<concept>
<code value="399244003"/>
<display value="Disorder of pituitary gland (disorder)"/>
</concept>
<concept>
<code value="190680002"/>
<display
value="Disorders of amino acid transport and metabolism (disorder)"/>
</concept>
<concept>
<code value="16652001"/>
<display value="Fabry's disease (disorder)"/>
</concept>
<concept>
<code value="79935000"/>
<display value="Farber's lipogranulomatosis (disorder)"/>
</concept>
<concept>
<code value="717276003"/>
<display value="Folinic acid responsive seizure syndrome (disorder)"/>
</concept>
<concept>
<code value="20052008"/>
<display
value="Fructose-1,6-bisphosphate aldolase B deficiency (disorder)"/>
</concept>
<concept>
<code value="28183005"/>
<display value="Fructose-biphosphatase deficiency (disorder)"/>
</concept>
<concept>
<code value="190745006"/>
<display value="Galactosemia (disorder)"/>
</concept>
<concept>
<code value="192782005"/>
<display
value="Galactosylceramide beta-galactosidase deficiency (disorder)"/>
</concept>
<concept>
<code value="190794006"/>
<display value="Glucosylceramide beta-glucosidase deficiency (disorder)"/>
</concept>
<concept>
<code value="235908005"/>
<display value="Glycogen storage disease type IX (disorder)"/>
</concept>
<concept>
<code value="41527003"/>
<display value="Glycogen storage disease type VIII (disorder)"/>
</concept>
<concept>
<code value="37666005"/>
<display value="Glycogen storage disease type X (disorder)"/>
</concept>
<concept>
<code value="717821004"/>
<display
value="Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder)"/>
</concept>
<concept>
<code value="7265005"/>
<display value="Glycogen storage disease, type I (disorder)"/>
</concept>
<concept>
<code value="274864009"/>
<display value="Glycogen storage disease, type II (disorder)"/>
</concept>
<concept>
<code value="66937008"/>
<display value="Glycogen storage disease, type III (disorder)"/>
</concept>
<concept>
<code value="11179002"/>
<display value="Glycogen storage disease, type IV (disorder)"/>
</concept>
<concept>
<code value="55912009"/>
<display value="Glycogen storage disease, type V (disorder)"/>
</concept>
<concept>
<code value="29291001"/>
<display value="Glycogen storage disease, type VI (disorder)"/>
</concept>
<concept>
<code value="89597008"/>
<display value="Glycogen storage disease, type VII (disorder)"/>
</concept>
<concept>
<code value="237964009"/>
<display value="Glycogen synthase deficiency (disorder)"/>
</concept>
<concept>
<code value="61598006"/>
<display value="Glycogenosis with glucoaminophosphaturia (disorder)"/>
</concept>
<concept>
<code value="238025006"/>
<display value="GM1 gangliosidosis (disorder)"/>
</concept>
<concept>
<code value="353295004"/>
<display value="Graves' disease (disorder)"/>
</concept>
<concept>
<code value="21983002"/>
<display value="Hashimoto thyroiditis (disorder)"/>
</concept>
<concept>
<code value="111578003"/>
<display
value="Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)"/>
</concept>
<concept>
<code value="66999008"/>
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