Family history of congenital disease (situation)
| Code | 160417009 |
|---|---|
| Semantic tag | situation |
| Module | international |
| Definition | defined |
| Effective time | 20040731 |
281666001Family history of disorder
situation
160389004FH: Polycystic kidney
situation
160320002FH: Sickle cell anaemia
situation
160321003FH: Sickle cell trait
situation
160319008FH: Thalassaemia
situation
64971000119106Family history of Von Hippel-Lindau syndrome
situation
431912005Family history of alpha-1-antitrypsin deficiency
situation
160425006Family history of chromosomal anomaly
situation
50050161000188101Family history of congenital immunodeficiency disease
situation
597941000005106Family history of congenital malformation
situation
64251000119106Family history of glycogen storage disease
situation
64391000119106Family history of haemoglobinopathy E
situation
64171000119108Family history of lysosomal storage disease
situation
65021000119105Family history of neurofibromatosis
situation
64161000119102Family history of phenylketonuria
situation
417001009Family history of tuberous sclerosis
situation