Logica COVID-19 FHIR Profile Library IG
0.10.1 - CI Build

Logica COVID-19 FHIR Profile Library IG - Local Development build (v0.10.1). See the Directory of published versions

COVID-19 metabolic underlying condition reference set

Summary

Defining URL:http://fhir.logicahealth.org/covid19/ValueSet/covid19-underlying-metabolic-condition-value-set
Version:0.10.1
Name:COVID19UnderlyingMetabolicConditionVS
Status:Active
Title:COVID-19 metabolic underlying condition reference set
Definition:

A set of codes that describe underlying metabolic conditions for COVID19

Publisher:Logica
Source Resource:XML / JSON / Turtle

References

Content Logical Definition

Logical Definition (CLD)

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

 

Expansion

This value set contains 96 concepts

Expansion based on SNOMED CT International edition 09-Mar 2020

All codes from system http://snomed.info/sct

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

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
Source The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code