Familial disease

Code	`111941005`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20020131

733650000Adult familial nephronophthisis with spastic quadriparesia syndrome disorder

773738009Chronic Epstein-Barr virus infection syndrome disorder

234576008Chronic familial neutropaenia disorder

236759008Congenital familial idiopathic priapism disorder

230265002Familial Alzheimer's disease of early onset disorder

721219005Familial Alzheimer-like prion disease disorder

39674000Familial C3B inhibitor deficiency syndrome disorder

722949001Familial Ménière disease disorder

715364001Familial abdominal aortic aneurysm disorder

235730004Familial absence of villi disorder

723359002Familial acute necrotising encephalopathy disorder

782917007Familial adrenal hypoplasia with absent pituitary luteinising hormone disorder

37495007Familial adrenocortical hypoplasia disorder

15123008Familial amyloid nephropathy with urticaria AND deafness disorder

42295001Familial amyloid polyneuropathy disorder

62216007Familial arthrogryposis-cholestatic hepatorenal syndrome disorder

715395008Familial atrial fibrillation disorder

1197418004Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease disorder

763531001Familial benign copper deficiency disorder

35728003Familial cardiomyopathy disorder

703226008Familial cerebral saccular aneurysm disorder

239840000Familial chondrocalcinosis disorder

726628003Familial chondromalacia of patella disorder

235073000Familial chronic mucocutaneous candidiasis disorder

1197489003Familial chylomicronemia syndrome disorder

784348007Familial congenital mirror movements disorder

1230016009Familial congenital nasolacrimal duct obstruction disorder

782679002Familial congenital palsy of trochlear nerve disorder

763770005Familial cortical myoclonus disorder

782823001Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome disorder

721220004Familial developmental dysphasia disorder

58618005Familial disease with storage of sterols (other than cholesterol) disorder

16516008Familial duodenal ulcer associated with rapid gastric emptying disorder

237547004Familial dysalbuminaemic hyperthyroxinaemia disorder

237554005Familial dyshormonogenetic goitre disorder

782756008Familial episodic pain syndrome disorder

230432008Familial febrile convulsions disorder

361200005Familial febrile urticaria disorder

233737004Familial fibrous mediastinitis disorder

703309000Familial gestational hyperthyroidism disorder

399094007Familial haematuria disorder

722721004Familial haemolytic uraemic syndrome disorder

398250003Familial haemophagocytic lymphohistiocytosis disorder

6935003Familial haemorrhagic diathesis disorder

95656000Familial hemiplegic migraine disorder

432726005Familial hirsutism disorder

15771000119109Familial hyperalphalipoproteinaemia disorder

723360007Familial hypercholanemia disorder

6761005Familial hypergastrinaemic duodenal ulcer disorder

1296480005Familial hyperinsulinemic hypoglycaemia disorder

763715007Familial hyperprolactinaemia disorder

1217069000Familial hyperreninaemic hypoaldosteronism type 1B disorder

722942005Familial hyperthyroidism disorder

721838005Familial hypertryptophanaemia disorder

715343000Familial hypoaldosteronism disorder

109447008Familial hypodontia disorder

81987005Familial hypokalaemic alkalosis, Gullner type disorder

716773002Familial idiopathic dilatation of right atrium disorder

237886009Familial idiopathic hypercalciuria disorder

426437004Familial idiopathic pulmonary fibrosis disorder

445404003Familial immunoglobulin A nephropathy disorder

784342008Familial infantile myoclonic epilepsy disorder

253789002Familial intestinal malrotation disorder

763691008Familial isolated clinodactyly of finger disorder

726708009Familial isolated congenital asplenia disorder

764523004Familial isolated trichomegaly disorder

46785007Familial juvenile hyperuricaemic nephropathy disorder

1264565005Familial lecithin cholesterol acyltransferase deficiency disorder

1279836009Familial multinodular goitre syndrome disorder

766888002Familial multiple lipomatosis disorder

763714006Familial multiple naevi flammei disorder

763532008Familial nasal acilia disorder

55352002Familial neoplastic disease disorder

237868006Familial non-neuropathic amyloidosis disorder

707208009Familial non-obstructive reflux-associated chronic pyelonephritis disorder

290439001Familial obesity disorder

715899006Familial osteochondritis dissecans disorder

773278003Familial osteodysplasia Anderson type disorder

403793002Familial painful callosities disorder

240133009Familial paroxysmal rhabdomyolysis disorder

1179298002Familial patent arterial duct disorder

716744000Familial penile hypospadias disorder

74381009Familial pericarditis disorder

238783008Familial pigmented purpuric eruption disorder

59229005Familial porphyria cutanea tarda disorder

236460004Familial proximal renal tubular acidosis disorder

402335001Familial psoriasis disorder

234161007Familial pulmonary capillary haemangiomatosis disorder

783257005Familial recurrent peripheral facial palsy disorder

75652008Familial renal iminoglycinuria disorder

766927009Familial supernumerary nipple disorder

783739005Familial temporal lobe epilepsy disorder

764965000Familial thoracic aortic aneurysm and aortic dissection disorder

783256001Familial thrombomodulin anomalies disorder

42021008Familial vasopressin-related polyuria disorder

763716008Familial vesicoureteral reflux disorder

69971003Haber's syndrome disorder

402459005Heredofamilial systemic amyloidosis affecting skin disorder

230318005Idiopathic familial dystonia disorder

48655003Isolated familial renal hypomagnesaemia disorder

76338009Normopepsinogenaemic familial duodenal ulcer disorder

764452004Retinal arterial macroaneurysm with supravalvular pulmonic stenosis disorder

55166000Thiemann disease familial form disorder

Parents (1)

Children (103)