FHIR IG analytics| Package | us.cdc.phinvads |
| Resource Type | ValueSet |
| Id | ValueSet-1.3.6.1.4.1.19376.1.7.3.1.1.23.8.13.json |
| FHIR Version | R4 |
| 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 codes used in this IG |
No narrative content found in resource
FHIR
FHIRsmith{
"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)"
}
]
}
]
}
}