Code
|
Display
|
86268005
|
Achondroplasia (disorder) |
63702009
|
Alstrom syndrome (disorder) |
195967001
|
Asthma (disorder) |
5619004
|
Bardet-Biedl syndrome (disorder) |
81780002
|
Beckwith-Wiedemann syndrome (disorder) |
162863004
|
Body mass index 25-29 - overweight (finding) |
162864005
|
Body mass index 30+ - obesity (finding) |
21634003
|
Borjeson-Forssman-Lehmann syndrome (disorder) |
405617006
|
Cardiovascular event (event) |
205813009
|
Carpenter's syndrome (disorder) |
128188000
|
Cerebral palsy (disorder) |
444862003
|
Childhood obesity (disorder) |
56604005
|
Cohen syndrome (disorder) |
41040004
|
Complete trisomy 21 syndrome (disorder) |
40354009
|
De Lange syndrome (disorder) |
35489007
|
Depressive disorder (disorder) |
73211009
|
Diabetes mellitus |
44054006
|
Diabetes mellitus type 2 (disorder) |
81531005
|
Diabetes mellitus type 2 in obese (disorder) |
46635009
|
Diabetes mellitus type I |
362969004
|
Disorder of endocrine system (disorder) |
39621005
|
Disorder of gallbladder (disorder) |
48606007
|
Drug resistance to insulin (disorder) |
185797004
|
Dwarfism (disorder) |
19155002
|
Dysfunctional uterine bleeding (finding) |
370992007
|
Dyslipidemia (disorder) |
266599000
|
Dysmenorrhea (disorder) |
72366004
|
Eating disorder (disorder) |
24203005
|
Extreme insulin resistance with acanthosis nigricans, hirsutism AND abnormal insulin receptors (disorder) |
20678000
|
Extreme insulin resistance with acanthosis nigricans, hirsutism AND autoantibodies to the insulin receptors (disorder) |
432726005
|
Familial hirsutism (disorder) |
290439001
|
Familial obesity (disorder) |
233944003
|
Familial primary pulmonary hypertension (disorder) |
433442009
|
Family history of bariatric operative procedure (situation) |
430091005
|
Family history of coronary arteriosclerosis (situation) |
160362009
|
Family history: Atherosclerosis (situation) |
266894000
|
Family history: Cardiovascular disease (situation) |
160394004
|
Family history: Early menarche (situation) |
160357008
|
Family history: Hypertension (situation) |
160311006
|
Family history: Obesity (situation) |
160401003
|
Family history: Raised blood pressure in pregnancy (situation) |
237793004
|
Hyperandrogenization syndrome (disorder) |
47270006
|
Hypercortisolism (disorder) |
81891001
|
Hypersecretion of ovarian androgens (disorder) |
82793005
|
Hypothalamic obesity (disorder) |
40930008
|
Hypothyroidism (disorder) |
71922006
|
Immune defect (finding) |
237651005
|
Insulin resistance - type A (disorder) |
237652003
|
Insulin resistance - type B (disorder) |
237650006
|
Insulin resistance in diabetes (disorder) |
237599002
|
Insulin-treated non-insulin-dependent diabetes mellitus (disorder) |
42681006
|
Islet cell hyperplasia (disorder) |
19346006
|
Marfan's syndrome (disorder) |
444161008
|
Maternal history of insulin dependence (situation) |
80660001
|
Mauriac's syndrome (disorder) |
74732009
|
Mental disorder (disorder) |
237602007
|
Metabolic syndrome X (disorder) |
55342001
|
Neoplastic disease (disorder) |
254264002
|
Partial trisomy 21 in Down's syndrome (disorder) |
360337007
|
PHHI - Persistent hyperinsulinemic hypoglycemia of infancy (disorder) |
69878008
|
Polycystic ovaries (disorder) |
89392001
|
Prader-Willi syndrome (disorder) |
400179000
|
Precocious puberty (disorder) |
237627000
|
Pregnancy and non-insulin-dependent diabetes mellitus (disorder) |
103021001
|
Premature adrenarche (finding) |
58833000
|
Pseudohypoparathyroidism type I A (disorder) |
68618008
|
Rett's disorder (disorder) |
37355009
|
Royer's syndrome (disorder) |
45582004
|
Rubinstein-Taybi syndrome (disorder) |
67531005
|
Spina bifida (disorder) |
442191002
|
Steatohepatitis (disorder) |
66214007
|
Substance abuse (disorder) |
371045000
|
Translocation Down syndrome (disorder) |
38804009
|
Turner syndrome (disorder) |
232057003
|
Usher syndrome type 1 (disorder) |
63247009
|
Williams syndrome (disorder) |