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111941005: Familial disease (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
179087019 Familial disease en Synonym Active Case insensitive SNOMED CT core
635166017 Familial disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core


157 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial disease Is a Disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial chronic mucocutaneous candidiasis Is a True Familial disease Inferred relationship Some
Familial osteodysplasia Anderson type Is a True Familial disease Inferred relationship Some
Chronic Epstein-Barr virus infection syndrome Is a True Familial disease Inferred relationship Some
Familial cervical artery dissection Is a True Familial disease Inferred relationship Some
Familial IgA nephropathy Is a True Familial disease Inferred relationship Some
Familial congenital palsy of trochlear nerve Is a True Familial disease Inferred relationship Some
Familial episodic pain syndrome Is a True Familial disease Inferred relationship Some
Familial adrenal hypoplasia with absent pituitary luteinising hormone Is a True Familial disease Inferred relationship Some
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome Is a True Familial disease Inferred relationship Some
Familial recurrent peripheral facial palsy Is a True Familial disease Inferred relationship Some
Familial thrombomodulin anomalies Is a True Familial disease Inferred relationship Some
Familial temporal lobe epilepsy Is a True Familial disease Inferred relationship Some
Familial congenital mirror movements Is a True Familial disease Inferred relationship Some
Familial infantile myoclonic epilepsy Is a True Familial disease Inferred relationship Some
Familial mesial temporal lobe epilepsy with febrile seizures Is a False Familial disease Inferred relationship Some
Autosomal dominant epilepsy with auditory features Is a True Familial disease Inferred relationship Some
Familial pulmonary capillary haemangiomatosis Is a True Familial disease Inferred relationship Some
Familial absence of villi Is a True Familial disease Inferred relationship Some
Heredofamilial systemic amyloidosis affecting skin Is a True Familial disease Inferred relationship Some
Familial haematuria Is a True Familial disease Inferred relationship Some
Isolated familial renal hypomagnesaemia Is a True Familial disease Inferred relationship Some
Familial non-neuropathic amyloidosis Is a True Familial disease Inferred relationship Some
Familial penile hypospadias Is a True Familial disease Inferred relationship Some
Familial osteoarthropathy of the fingers Is a True Familial disease Inferred relationship Some
Familial pigmented purpuric eruption Is a True Familial disease Inferred relationship Some
Familial fibrous mediastinitis Is a True Familial disease Inferred relationship Some
Familial gestational hyperthyroidism Is a True Familial disease Inferred relationship Some
Haber's syndrome Is a True Familial disease Inferred relationship Some
Familial osteochondritis dissecans Is a True Familial disease Inferred relationship Some
Familial idiopathic hypercalciuria Is a True Familial disease Inferred relationship Some
Idiopathic familial dystonia Is a True Familial disease Inferred relationship Some
Familial paroxysmal rhabdomyolysis Is a True Familial disease Inferred relationship Some
Familial obesity Is a True Familial disease Inferred relationship Some
Glomerular disease due to familial disease Due to True Familial disease Inferred relationship Some 2
Familial dyshormonogenetic goitre Is a True Familial disease Inferred relationship Some
Familial patent arterial duct Is a True Familial disease Inferred relationship Some
Familial hyperreninaemic hypoaldosteronism type 2 Is a False Familial disease Inferred relationship Some
Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease Is a True Familial disease Inferred relationship Some
Familial chylomicronemia syndrome Is a True Familial disease Inferred relationship Some
Familial cerebral saccular aneurysm Is a True Familial disease Inferred relationship Some
Familial hyperreninaemic hypoaldosteronism type 1B Is a True Familial disease Inferred relationship Some
Familial congenital nasolacrimal duct obstruction Is a True Familial disease Inferred relationship Some
Familial intestinal malrotation Is a True Familial disease Inferred relationship Some
Familial juvenile gout Is a True Familial disease Inferred relationship Some
Familial restrictive cardiomyopathy Is a False Familial disease Inferred relationship Some
Familial dysalbuminaemic hyperthyroxinaemia Is a True Familial disease Inferred relationship Some
Familial hypergastrinaemic duodenal ulcer Is a True Familial disease Inferred relationship Some
Familial amyloid nephropathy with urticaria AND deafness Is a True Familial disease Inferred relationship Some
Familial febrile urticaria Is a True Familial disease Inferred relationship Some
Familial duodenal ulcer associated with rapid gastric emptying Is a True Familial disease Inferred relationship Some
Maturity onset diabetes mellitus in young Is a False Familial disease Inferred relationship Some
Familial cardiomyopathy Is a True Familial disease Inferred relationship Some
Familial adrenocortical hypoplasia Is a True Familial disease Inferred relationship Some
Familial C3B inhibitor deficiency syndrome Is a True Familial disease Inferred relationship Some
Familial amyloid polyneuropathy Is a True Familial disease Inferred relationship Some
Familial painful callosities Is a True Familial disease Inferred relationship Some
Hereditary motor neuron disease Is a False Familial disease Inferred relationship Some
Cherubism Is a False Familial disease Inferred relationship Some
Peutz-Jeghers syndrome Is a False Familial disease Inferred relationship Some
Familial neoplastic disease Is a True Familial disease Inferred relationship Some
Familial disease with storage of sterols (other than cholesterol) Is a True Familial disease Inferred relationship Some
Familial arthrogryposis-cholestatic hepatorenal syndrome Is a True Familial disease Inferred relationship Some
Familial haemorrhagic diathesis Is a True Familial disease Inferred relationship Some
Familial neonatal seizures Is a True Familial disease Inferred relationship Some
Familial multiple polyposis syndrome Is a False Familial disease Inferred relationship Some
Familial renal iminoglycinuria Is a True Familial disease Inferred relationship Some
Normopepsinogenaemic familial duodenal ulcer Is a True Familial disease Inferred relationship Some
Chronic familial neutropenia Is a True Familial disease Inferred relationship Some
Familial hypokalaemic alkalosis, Gullner type Is a True Familial disease Inferred relationship Some
Familial hemiplegic migraine Is a True Familial disease Inferred relationship Some
Familial idiopathic pulmonary fibrosis Is a True Familial disease Inferred relationship Some
Familial hirsutism Is a True Familial disease Inferred relationship Some
Familial hypodontia Is a True Familial disease Inferred relationship Some
Familial febrile convulsions Is a True Familial disease Inferred relationship Some
Familial Alzheimer's disease of early onset Is a True Familial disease Inferred relationship Some
Familial hyperalphalipoproteinaemia Is a True Familial disease Inferred relationship Some
Familial non-obstructive reflux-associated chronic pyelonephritis Is a True Familial disease Inferred relationship Some
Congenital familial idiopathic priapism Is a True Familial disease Inferred relationship Some
Familial hypoaldosteronism Is a True Familial disease Inferred relationship Some
Familial abdominal aortic aneurysm Is a True Familial disease Inferred relationship Some
Familial atrial fibrillation Is a True Familial disease Inferred relationship Some
Familial idiopathic dilatation of right atrium Is a True Familial disease Inferred relationship Some
Familial Alzheimer-like prion disease Is a True Familial disease Inferred relationship Some
Familial developmental dysphasia Is a True Familial disease Inferred relationship Some
Hyperinsulinism due to insulin receptor deficiency Is a True Familial disease Inferred relationship Some
Familial hypertryptophanaemia Is a True Familial disease Inferred relationship Some
Familial haemolytic uraemic syndrome Is a True Familial disease Inferred relationship Some
Familial hyperthyroidism Is a True Familial disease Inferred relationship Some
Familial Ménière disease Is a True Familial disease Inferred relationship Some
Familial acute necrotising encephalopathy Is a True Familial disease Inferred relationship Some
Familial hypercholanemia Is a True Familial disease Inferred relationship Some
Familial isolated congenital asplenia Is a True Familial disease Inferred relationship Some
Familial porphyria cutanea tarda Is a True Familial disease Inferred relationship Some
Adult familial nephronophthisis with spastic quadriparesia syndrome Is a True Familial disease Inferred relationship Some
Familial pericarditis Is a True Familial disease Inferred relationship Some
Familial benign copper deficiency Is a True Familial disease Inferred relationship Some
Familial nasal acilia Is a True Familial disease Inferred relationship Some
Familial multiple naevi flammei Is a True Familial disease Inferred relationship Some
Familial hyperprolactinaemia Is a True Familial disease Inferred relationship Some
Familial vesicoureteral reflux Is a True Familial disease Inferred relationship Some
Familial isolated clinodactyly of finger Is a True Familial disease Inferred relationship Some

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Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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