Family history of hereditary disease

160318000FH: Hereditary spherocytosis situation

160336000FH: Huntington's chorea situation

160320002FH: Sickle cell anaemia situation

160321003FH: Sickle cell trait situation

160319008FH: Thalassaemia situation

98251000119101Family history of Canavan disease situation

429970002Family history of Charcot-Marie-Tooth disease situation

65031000119108Family history of Cowden syndrome situation

64181000119106Family history of Marfan syndrome situation

63921000119108Family history of Rett syndrome situation

63931000119106Family history of Steinert myotonic dystrophy situation

64971000119106Family history of Von Hippel-Lindau syndrome situation

64121000119107Family history of achondroplasia situation

431912005Family history of alpha-1-antitrypsin deficiency situation

1269318001Family history of congenital long QT syndrome situation

160309002Family history of cystic fibrosis situation

109271000119105Family history of double heterozygous familial hypercholesterolaemia situation

94691000119101Family history of familial dysautonomia situation

709090007Family history of familial multiple polyposis syndrome situation

65071000119106Family history of fragile X syndrome situation

64251000119106Family history of glycogen storage disease situation

64391000119106Family history of haemoglobinopathy E situation

218432961000119106Family history of hereditary diffuse gastric cancer situation

1098871000119109Family history of hereditary nonpolyposis colon cancer situation

81651000119109Family history of heritable malignancy situation

64171000119108Family history of lysosomal storage disease situation

64161000119102Family history of phenylketonuria situation

109011000119108Family history of protein C resistance situation

71271000119107Family history of retinitis pigmentosa situation

63881000119101Family history of spinocerebellar ataxia situation

417001009Family history of tuberous sclerosis situation

Synonyms