Family history of metabolic disorder (situation)
| Code | 160305008 |
|---|---|
| Semantic tag | situation |
| Module | international |
| Definition | defined |
| Effective time | 20040731 |
281666001Family history of disorder
situation
160402005FH: Diabetes in pregnancy
situation
160308005FH: Gout
situation
199071000000106FH: Lactose intolerance
situation
821691000000104FH: MCADD (medium chain acyl coenzyme A dehydrogenase deficiency)
situation
160310007FH: Porphyria
situation
98251000119101Family history of Canavan disease
situation
789240000Family history of acetylcholinesterase deficiency
situation
431912005Family history of alpha-1-antitrypsin deficiency
situation
98011000119108Family history of butyrylcholinesterase deficiency
situation
160303001Family history of diabetes mellitus
situation
64081000119105Family history of galactosaemia
situation
64251000119106Family history of glycogen storage disease
situation
401119001Family history of haemochromatosis
situation
74131000119101Family history of hyperbetalipoproteinaemia
situation
725117008Family history of hyperlipidaemia
situation
74171000119103Family history of hypoalphalipoproteinaemia
situation
429971003Family history of impaired glucose tolerance
situation
1264214003Family history of lipoprotein (a) hyperlipoproteinaemia
situation
64171000119108Family history of lysosomal storage disease
situation
64131000119105Family history of methylmalonic aciduria
situation
473070008Family history of mitochondrial disease
situation
64161000119102Family history of phenylketonuria
situation
781073000Family history of polycystic ovary syndrome
situation
1102141000000105Family history of thyrotoxicosis
situation