Package | us.cdc.phinvads |
Resource Type | ValueSet |
Id | 1.3.6.1.4.1.19376.1.7.3.1.1.23.8.13 |
FHIR Version | R4 |
Source | http://fhir.org/packages/us.cdc.phinvads |
URL | http://phinvads.cdc.gov/fhir/ValueSet/1.3.6.1.4.1.19376.1.7.3.1.1.23.8.13 |
Version | 1 |
Status | active |
Date | 2014-01-06T00:03:00+11:00 |
Name | PHVS_FamilyHistory_HW |
Title | Family History (HW) |
Realm | us |
Description | To reflect Family History that impact Healthy Weight |
No resources found
CodeSystem | |
sct | SNOMED CT (all versions) |
No narrative content found in resource
{ "resourceType": "ValueSet", "id": "1.3.6.1.4.1.19376.1.7.3.1.1.23.8.13", "meta": { "source": "https://phinvads.cdc.gov/vads/ViewValueSet.action?oid=1.3.6.1.4.1.19376.1.7.3.1.1.23.8.13" }, "url": "http://phinvads.cdc.gov/fhir/ValueSet/1.3.6.1.4.1.19376.1.7.3.1.1.23.8.13", "version": "1", "name": "PHVS_FamilyHistory_HW", "title": "Family History (HW)", "status": "active", "date": "2014-01-06T00:03:00+11:00", "description": "To reflect Family History that impact Healthy Weight", "compose": { "include": [ { "system": "http://snomed.info/sct", "version": "http://snomed.info/sct/731000124108/version/20200901", "concept": [ { "code": "86268005", "display": "Achondroplasia (disorder)" }, { "code": "63702009", "display": "Alstrom syndrome (disorder)" }, { "code": "195967001", "display": "Asthma (disorder)" }, { "code": "5619004", "display": "Bardet-Biedl syndrome (disorder)" }, { "code": "81780002", "display": "Beckwith-Wiedemann syndrome (disorder)" }, { "code": "162863004", "display": "Body mass index 25-29 - overweight (finding)" }, { "code": "162864005", "display": "Body mass index 30+ - obesity (finding)" }, { "code": "21634003", "display": "Borjeson-Forssman-Lehmann syndrome (disorder)" }, { "code": "405617006", "display": "Cardiovascular event (event)" }, { "code": "205813009", "display": "Carpenter's syndrome (disorder)" }, { "code": "128188000", "display": "Cerebral palsy (disorder)" }, { "code": "444862003", "display": "Childhood obesity (disorder)" }, { "code": "56604005", "display": "Cohen syndrome (disorder)" }, { "code": "41040004", "display": "Complete trisomy 21 syndrome (disorder)" }, { "code": "40354009", "display": "De Lange syndrome (disorder)" }, { "code": "35489007", "display": "Depressive disorder (disorder)" }, { "code": "73211009", "display": "Diabetes mellitus" }, { "code": "44054006", "display": "Diabetes mellitus type 2 (disorder)" }, { "code": "81531005", "display": "Diabetes mellitus type 2 in obese (disorder)" }, { "code": "46635009", "display": "Diabetes mellitus type I" }, { "code": "362969004", "display": "Disorder of endocrine system (disorder)" }, { "code": "39621005", "display": "Disorder of gallbladder (disorder)" }, { "code": "48606007", "display": "Drug resistance to insulin (disorder)" }, { "code": "185797004", "display": "Dwarfism (disorder)" }, { "code": "19155002", "display": "Dysfunctional uterine bleeding (finding)" }, { "code": "370992007", "display": "Dyslipidemia (disorder)" }, { "code": "266599000", "display": "Dysmenorrhea (disorder)" }, { "code": "72366004", "display": "Eating disorder (disorder)" }, { "code": "24203005", "display": "Extreme insulin resistance with acanthosis nigricans, hirsutism AND abnormal insulin receptors (disorder)" }, { "code": "20678000", "display": "Extreme insulin resistance with acanthosis nigricans, hirsutism AND autoantibodies to the insulin receptors (disorder)" }, { "code": "432726005", "display": "Familial hirsutism (disorder)" }, { "code": "290439001", "display": "Familial obesity (disorder)" }, { "code": "233944003", "display": "Familial primary pulmonary hypertension (disorder)" }, { "code": "433442009", "display": "Family history of bariatric operative procedure (situation)" }, { "code": "430091005", "display": "Family history of coronary arteriosclerosis (situation)" }, { "code": "160362009", "display": "Family history: Atherosclerosis (situation)" }, { "code": "266894000", "display": "Family history: Cardiovascular disease (situation)" }, { "code": "160394004", "display": "Family history: Early menarche (situation)" }, { "code": "160357008", "display": "Family history: Hypertension (situation)" }, { "code": "160311006", "display": "Family history: Obesity (situation)" }, { "code": "160401003", "display": "Family history: Raised blood pressure in pregnancy (situation)" }, { "code": "237793004", "display": "Hyperandrogenization syndrome (disorder) " }, { "code": "47270006", "display": "Hypercortisolism (disorder)" }, { "code": "81891001", "display": "Hypersecretion of ovarian androgens (disorder)" }, { "code": "82793005", "display": "Hypothalamic obesity (disorder)" }, { "code": "40930008", "display": "Hypothyroidism (disorder)" }, { "code": "71922006", "display": "Immune defect (finding)" }, { "code": "237651005", "display": "Insulin resistance - type A (disorder)" }, { "code": "237652003", "display": "Insulin resistance - type B (disorder)" }, { "code": "237650006", "display": "Insulin resistance in diabetes (disorder)" }, { "code": "237599002", "display": "Insulin-treated non-insulin-dependent diabetes mellitus (disorder)" }, { "code": "42681006", "display": "Islet cell hyperplasia (disorder) " }, { "code": "19346006", "display": "Marfan's syndrome (disorder)" }, { "code": "444161008", "display": "Maternal history of insulin dependence (situation)" }, { "code": "80660001", "display": "Mauriac's syndrome (disorder)" }, { "code": "74732009", "display": "Mental disorder (disorder)" }, { "code": "237602007", "display": "Metabolic syndrome X (disorder)" }, { "code": "55342001", "display": "Neoplastic disease (disorder) " }, { "code": "254264002", "display": "Partial trisomy 21 in Down's syndrome (disorder)" }, { "code": "360337007", "display": "PHHI - Persistent hyperinsulinemic hypoglycemia of infancy (disorder) " }, { "code": "69878008", "display": "Polycystic ovaries (disorder)" }, { "code": "89392001", "display": "Prader-Willi syndrome (disorder)" }, { "code": "400179000", "display": "Precocious puberty (disorder)" }, { "code": "237627000", "display": "Pregnancy and non-insulin-dependent diabetes mellitus (disorder)" }, { "code": "103021001", "display": "Premature adrenarche (finding) " }, { "code": "58833000", "display": "Pseudohypoparathyroidism type I A (disorder) " }, { "code": "68618008", "display": "Rett's disorder (disorder)" }, { "code": "37355009", "display": "Royer's syndrome (disorder)" }, { "code": "45582004", "display": "Rubinstein-Taybi syndrome (disorder)" }, { "code": "67531005", "display": "Spina bifida (disorder)" }, { "code": "442191002", "display": "Steatohepatitis (disorder)" }, { "code": "66214007", "display": "Substance abuse (disorder)" }, { "code": "371045000", "display": "Translocation Down syndrome (disorder)" }, { "code": "38804009", "display": "Turner syndrome (disorder)" }, { "code": "232057003", "display": "Usher syndrome type 1 (disorder)" }, { "code": "63247009", "display": "Williams syndrome (disorder)" } ] } ] } }