## ValueSet Comparison between http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-metabolic-condition-value-set vs http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-metabolic-condition-value-set

### Messages

Error | ValueSet.version | Values for version differ: '0.14.0' vs '1.0.0'
Information | ValueSet.date | Values for date differ: '2021-12-08T02:47:19+00:00' vs '2022-07-25T13:34:17+00:00'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Chronic metabolic disorder (disorder)' vs 'Chronic metabolic disorder (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Diabetes mellitus (disorder)' vs 'Diabetes mellitus (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Disorder of adrenal gland (disorder)' vs 'Disorder of adrenal gland (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Disorder of parathyroid gland (disorder)' vs 'Disorder of parathyroid gland (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Disorder of pituitary gland (disorder)' vs 'Disorder of pituitary gland (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Inborn error of metabolism (disorder)' vs 'Inborn error of metabolism (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Metabolic syndrome X (disorder)' vs 'Metabolic syndrome X (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Storage disease (disorder)' vs 'Storage disease (disorder)'
Warning | ValueSet.expansion.contains.name | Changed value for display: 'Thyroid dysfunction (disorder)' vs 'Thyroid dysfunction (disorder)'

### Metadata

Name | Value | Comments
--- | --- | ---
compose.inactive |  |
compose.lockedDate |  |
copyright | This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement |
date | 2021-12-08T02:47:19+00:00 | 2022-07-25T13:34:17+00:00 | Values Differ
description | A set of codes that describe underlying metabolic conditions for COVID19 |
experimental |  |
immutable |  |
jurisdiction |  |
jurisdiction[0] | urn:iso:std:iso:3166#US |
name | COVID19UnderlyingMetabolicConditionVS |
publisher | HL7 International - Clinical Information Modeling Initiative |
purpose |  |
status | active |
title | COVID-19 metabolic underlying condition reference set |
url | http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-metabolic-condition-value-set |
version | 0.14.0 | 1.0.0 | Values Differ

### Definition

Item | Property | Value | Comments
--- | --- | --- | ---
include | http://snomed.info/sct |  |
Concept | 267454002 | Acatalasemia (disorder) |
Concept | 238069004 | Acyl-coenzyme A oxidase deficiency (disorder) |
Concept | 363732003 | Addison's disease (disorder) |
Concept | 386584007 | Adrenal cortical hypofunction (disorder) |
Concept | 237735008 | Adrenal Cushing's syndrome (disorder) |
Concept | 65389002 | Adrenoleukodystrophy (disorder) |
Concept | 700463002 | Alpha-methylacyl-CoA racemase deficiency disorder (disorder) |
Concept | 54954004 | Aspartylglucosaminuria (disorder) |
Concept | 238068007 | Bifunctional peroxisomal enzyme deficiency (disorder) |
Concept | 128289001 | Chronic metabolic disorder (disorder) | Chronic metabolic disorder (disorder) |
Concept | 7573000 | Classical phenylketonuria (disorder) |
Concept | 35691006 | Combined deficiency of sialidase AND beta galactosidase (disorder) |
Concept | 237751000 | Congenital adrenal hyperplasia (disorder) |
Concept | 419097006 | Danon disease (disorder) |
Concept | 124302001 | Deficiency of galactokinase (disorder) |
Concept | 124437004 | Deficiency of glucose-6-phosphatase (disorder) |
Concept | 124335006 | Deficiency of phosphoglycerate kinase (disorder) |
Concept | 124675005 | Deficiency of phosphoglycerate mutase (disorder) |
Concept | 387817006 | Deficiency of phosphorylase b kinase (disorder) |
Concept | 124329006 | Deficiency of phosphorylase kinase (disorder) |
Concept | 46635009 | Diabetes mellitus type 1 (disorder) |
Concept | 44054006 | Diabetes mellitus type 2 (disorder) |
Concept | 73211009 | Diabetes mellitus (disorder) | Diabetes mellitus (disorder) |
Concept | 45744005 | Disorder of mineral metabolism (disorder) |
Concept | 238059005 | Disorder of peroxisomal function (disorder) |
Concept | 238006008 | Disorder of purine and pyrimidine metabolism (disorder) |
Concept | 30171000 | Disorder of adrenal gland (disorder) | Disorder of adrenal gland (disorder) |
Concept | 73132005 | Disorder of parathyroid gland (disorder) | Disorder of parathyroid gland (disorder) |
Concept | 399244003 | Disorder of pituitary gland (disorder) | Disorder of pituitary gland (disorder) |
Concept | 190680002 | Disorders of amino acid transport and metabolism (disorder) |
Concept | 16652001 | Fabry's disease (disorder) |
Concept | 79935000 | Farber's lipogranulomatosis (disorder) |
Concept | 717276003 | Folinic acid responsive seizure syndrome (disorder) |
Concept | 20052008 | Fructose-1,6-bisphosphate aldolase B deficiency (disorder) |
Concept | 28183005 | Fructose-biphosphatase deficiency (disorder) |
Concept | 190745006 | Galactosemia (disorder) |
Concept | 192782005 | Galactosylceramide beta-galactosidase deficiency (disorder) |
Concept | 190794006 | Glucosylceramide beta-glucosidase deficiency (disorder) |
Concept | 235908005 | Glycogen storage disease type IX (disorder) |
Concept | 41527003 | Glycogen storage disease type VIII (disorder) |
Concept | 37666005 | Glycogen storage disease type X (disorder) |
Concept | 717821004 | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder) |
Concept | 7265005 | Glycogen storage disease, type I (disorder) |
Concept | 274864009 | Glycogen storage disease, type II (disorder) |
Concept | 66937008 | Glycogen storage disease, type III (disorder) |
Concept | 11179002 | Glycogen storage disease, type IV (disorder) |
Concept | 55912009 | Glycogen storage disease, type V (disorder) |
Concept | 29291001 | Glycogen storage disease, type VI (disorder) |
Concept | 89597008 | Glycogen storage disease, type VII (disorder) |
Concept | 237964009 | Glycogen synthase deficiency (disorder) |
Concept | 61598006 | Glycogenosis with glucoaminophosphaturia (disorder) |
Concept | 238025006 | GM1 gangliosidosis (disorder) |
Concept | 353295004 | Graves' disease (disorder) |
Concept | 21983002 | Hashimoto thyroiditis (disorder) |
Concept | 111578003 | Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) |
Concept | 66999008 | Hyperparathyroidism (disorder) |
Concept | 10649000 | Hyperpituitarism (disorder) |
Concept | 34486009 | Hyperthyroidism (disorder) |
Concept | 36976004 | Hypoparathyroidism (disorder) |
Concept | 74728003 | Hypopituitarism (disorder) |
Concept | 40930008 | Hypothyroidism (disorder) |
Concept | 70199000 | I-cell disease (disorder) |
Concept | 86095007 | Inborn error of metabolism (disorder) | Inborn error of metabolism (disorder) |
Concept | 238062008 | Infantile Refsum's disease (disorder) |
Concept | 18756002 | Juvenile GM1 gangliosidosis (disorder) |
Concept | 65524005 | Mannosidosis (disorder) |
Concept | 27718001 | Maple syrup urine disease (disorder) |
Concept | 69463008 | Maroteaux-Lamy syndrome (disorder) |
Concept | 237602007 | Metabolic syndrome X (disorder) | Metabolic syndrome X (disorder) |
Concept | 396338004 | Metachromatic leucodystrophy (disorder) |
Concept | 725296006 | Mucolipidosis type IV (disorder) |
Concept | 75610003 | Mucopolysaccharidosis type I (disorder) |
Concept | 65327002 | Mucopolysaccharidosis type I-H (disorder) |
Concept | 26745009 | Mucopolysaccharidosis type I-H/S (disorder) |
Concept | 70737009 | Mucopolysaccharidosis type II (disorder) |
Concept | 73123008 | Mucopolysaccharidosis type I-S (disorder) |
Concept | 43916004 | Mucopolysaccharidosis type VII (disorder) |
Concept | 378007 | Morquio syndrome (disorder) |
Concept | 238061001 | Neonatal adrenoleucodystrophy (disorder) |
Concept | 783717008 | Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder) |
Concept | 5335002 | Phosphoenolpyruvate carboxykinase deficiency (disorder) |
Concept | 25362006 | Phytanic acid storage disease (disorder) |
Concept | 65520001 | Primary hyperoxaluria, type I (disorder) |
Concept | 65764006 | Pseudo-Hurler polydystrophy (disorder) |
Concept | 734434007 | Pyridoxine-dependent epilepsy (disorder) |
Concept | 46683007 | Pyruvate dehydrogenase complex deficiency (disorder) |
Concept | 23849003 | Sandhoff disease (disorder) |
Concept | 88393000 | Sanfilippo syndrome (disorder) |
Concept | 38795005 | Sialidosis (disorder) |
Concept | 58459009 | Sphingomyelin/cholesterol lipidosis (disorder) |
Concept | 34420000 | Storage disease (disorder) | Storage disease (disorder) |
Concept | 367368009 | Sulfite oxidase deficiency (disorder) |
Concept | 111385000 | Tay-Sachs disease (disorder) |
Concept | 264580006 | Thyroid dysfunction (disorder) | Thyroid dysfunction (disorder) |
Concept | 8849004 | Uridine diphosphate glucose-4-epimerase deficiency (disorder) |
Concept | 88469006 | Zellweger syndrome (disorder) |

### Expansion

Code | Display | Comments
--- | --- | ---
267454002 | Acatalasemia (disorder) |
238069004 | Acyl-coenzyme A oxidase deficiency (disorder) |
363732003 | Addison's disease (disorder) |
386584007 | Adrenal cortical hypofunction (disorder) |
237735008 | Adrenal Cushing's syndrome (disorder) |
65389002 | Adrenoleukodystrophy (disorder) |
700463002 | Alpha-methylacyl-CoA racemase deficiency disorder (disorder) |
54954004 | Aspartylglucosaminuria (disorder) |
238068007 | Bifunctional peroxisomal enzyme deficiency (disorder) |
128289001 | Chronic metabolic disorder (disorder) | Chronic metabolic disorder (disorder) | display changed from left to right
7573000 | Classical phenylketonuria (disorder) |
35691006 | Combined deficiency of sialidase AND beta galactosidase (disorder) |
237751000 | Congenital adrenal hyperplasia (disorder) |
419097006 | Danon disease (disorder) |
124302001 | Deficiency of galactokinase (disorder) |
124437004 | Deficiency of glucose-6-phosphatase (disorder) |
124335006 | Deficiency of phosphoglycerate kinase (disorder) |
124675005 | Deficiency of phosphoglycerate mutase (disorder) |
387817006 | Deficiency of phosphorylase b kinase (disorder) |
124329006 | Deficiency of phosphorylase kinase (disorder) |
46635009 | Diabetes mellitus type 1 (disorder) |
44054006 | Diabetes mellitus type 2 (disorder) |
73211009 | Diabetes mellitus (disorder) | Diabetes mellitus (disorder) | display changed from left to right
45744005 | Disorder of mineral metabolism (disorder) |
238059005 | Disorder of peroxisomal function (disorder) |
238006008 | Disorder of purine and pyrimidine metabolism (disorder) |
30171000 | Disorder of adrenal gland (disorder) | Disorder of adrenal gland (disorder) | display changed from left to right
73132005 | Disorder of parathyroid gland (disorder) | Disorder of parathyroid gland (disorder) | display changed from left to right
399244003 | Disorder of pituitary gland (disorder) | Disorder of pituitary gland (disorder) | display changed from left to right
190680002 | Disorders of amino acid transport and metabolism (disorder) |
16652001 | Fabry's disease (disorder) |
79935000 | Farber's lipogranulomatosis (disorder) |
717276003 | Folinic acid responsive seizure syndrome (disorder) |
20052008 | Fructose-1,6-bisphosphate aldolase B deficiency (disorder) |
28183005 | Fructose-biphosphatase deficiency (disorder) |
190745006 | Galactosemia (disorder) |
192782005 | Galactosylceramide beta-galactosidase deficiency (disorder) |
190794006 | Glucosylceramide beta-glucosidase deficiency (disorder) |
235908005 | Glycogen storage disease type IX (disorder) |
41527003 | Glycogen storage disease type VIII (disorder) |
37666005 | Glycogen storage disease type X (disorder) |
717821004 | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder) |
7265005 | Glycogen storage disease, type I (disorder) |
274864009 | Glycogen storage disease, type II (disorder) |
66937008 | Glycogen storage disease, type III (disorder) |
11179002 | Glycogen storage disease, type IV (disorder) |
55912009 | Glycogen storage disease, type V (disorder) |
29291001 | Glycogen storage disease, type VI (disorder) |
89597008 | Glycogen storage disease, type VII (disorder) |
237964009 | Glycogen synthase deficiency (disorder) |
61598006 | Glycogenosis with glucoaminophosphaturia (disorder) |
238025006 | GM1 gangliosidosis (disorder) |
353295004 | Graves' disease (disorder) |
21983002 | Hashimoto thyroiditis (disorder) |
111578003 | Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder) |
66999008 | Hyperparathyroidism (disorder) |
10649000 | Hyperpituitarism (disorder) |
34486009 | Hyperthyroidism (disorder) |
36976004 | Hypoparathyroidism (disorder) |
74728003 | Hypopituitarism (disorder) |
40930008 | Hypothyroidism (disorder) |
70199000 | I-cell disease (disorder) |
86095007 | Inborn error of metabolism (disorder) | Inborn error of metabolism (disorder) | display changed from left to right
238062008 | Infantile Refsum's disease (disorder) |
18756002 | Juvenile GM1 gangliosidosis (disorder) |
65524005 | Mannosidosis (disorder) |
27718001 | Maple syrup urine disease (disorder) |
69463008 | Maroteaux-Lamy syndrome (disorder) |
237602007 | Metabolic syndrome X (disorder) | Metabolic syndrome X (disorder) | display changed from left to right
396338004 | Metachromatic leucodystrophy (disorder) |
725296006 | Mucolipidosis type IV (disorder) |
75610003 | Mucopolysaccharidosis type I (disorder) |
65327002 | Mucopolysaccharidosis type I-H (disorder) |
26745009 | Mucopolysaccharidosis type I-H/S (disorder) |
70737009 | Mucopolysaccharidosis type II (disorder) |
73123008 | Mucopolysaccharidosis type I-S (disorder) |
43916004 | Mucopolysaccharidosis type VII (disorder) |
378007 | Morquio syndrome (disorder) |
238061001 | Neonatal adrenoleucodystrophy (disorder) |
783717008 | Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder) |
5335002 | Phosphoenolpyruvate carboxykinase deficiency (disorder) |
25362006 | Phytanic acid storage disease (disorder) |
65520001 | Primary hyperoxaluria, type I (disorder) |
65764006 | Pseudo-Hurler polydystrophy (disorder) |
734434007 | Pyridoxine-dependent epilepsy (disorder) |
46683007 | Pyruvate dehydrogenase complex deficiency (disorder) |
23849003 | Sandhoff disease (disorder) |
88393000 | Sanfilippo syndrome (disorder) |
38795005 | Sialidosis (disorder) |
58459009 | Sphingomyelin/cholesterol lipidosis (disorder) |
34420000 | Storage disease (disorder) | Storage disease (disorder) | display changed from left to right
367368009 | Sulfite oxidase deficiency (disorder) |
111385000 | Tay-Sachs disease (disorder) |
264580006 | Thyroid dysfunction (disorder) | Thyroid dysfunction (disorder) | display changed from left to right
8849004 | Uridine diphosphate glucose-4-epimerase deficiency (disorder) |
88469006 | Zellweger syndrome (disorder) |