Disease

Familial disease (disorder)
	Familial disease
	familiaire aandoening
	familiale ziekte

Id	111941005
Status	Primitive

PALGA thesaurus simple reference set for pathology

ICD-10 complex map reference set

Target
Rule	TRUE
Advice	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
Correlation	SNOMED CT source code to target map code correlation not specified

Adult familial nephronophthisis with spastic quadriparesia syndrome

Autosomal dominant epilepsy with auditory features

Autosomal recessive familial isolated hypoparathyroidism

Chronic Epstein-Barr virus infection syndrome

Chronic familial neutropenia Chronic familial neutropaenia

Congenital familial idiopathic priapism

Familial abdominal aortic aneurysm

Familial absence of villi

Familial acute necrotizing encephalopathy

Familial adrenal hypoplasia with absent pituitary luteinizing hormone

Familial adrenocortical hypoplasia

Familial adult vitelliform macular dystrophy

Familial Alzheimer's disease1

Familial Alzheimer's disease of early onset3

Familial Alzheimer-like prion disease

Familial amyloid nephropathy with urticaria AND deafness

Familial amyloid polyneuropathy6

Familial amyloidosis

Familial arthrogryposis-cholestatic hepatorenal syndrome

Familial atrial fibrillation

Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease

Familial autosomal dominant hypoparathyroidism

Familial benign copper deficiency

Familial C3B inhibitor deficiency syndrome

Familial cardiomyopathy6

Familial carpal tunnel syndrome

Familial cerebral saccular aneurysm

Familial cervical artery dissection

Familial chronic mucocutaneous candidiasis3

Familial chylomicronemia syndrome2

Familial congenital mirror movements

Familial congenital nasolacrimal duct obstruction

Familial congenital palsy of trochlear nerve

Familial cortical myoclonus

Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome

Familial delayed puberty

Familial dermatomyositis

Familial developmental dysphasia

Familial disease with storage of sterols (other than cholesterol)1

Familial duodenal ulcer associated with rapid gastric emptying

Familial dysalbuminemic hyperthyroxinemia

Familial dyshormonogenetic goiter

Familial episodic pain syndrome

Familial febrile convulsions1

Familial febrile urticaria

Familial fibrous mediastinitis

Familial gestational hyperthyroidism

Familial hematuria

Familial hemiplegic migraine

Familial hemolytic uremic syndrome

Familial hemophagocytic lymphohistiocytosis4

Familial hemorrhagic diathesis

Familial hirsutism

Familial hyperalphalipoproteinemia

Familial hypercalciuria

Familial hypercholanemia

Familial hypergastrinemic duodenal ulcer

Familial hyperprolactinemia

Familial hyperreninemic hypoaldosteronism type 1B

Familial hyperthyroidism

Familial hypertryptophanemia

Familial hypoaldosteronism2

Familial hypodontia

Familial hypokalemic alkalosis, Gullner type

Familial idiopathic dilatation of right atrium

Familial idiopathic hypercalciuria

Familial idiopathic pulmonary fibrosis

Familial immunoglobulin A nephropathy

Familial infantile myoclonic epilepsy

Familial intestinal malrotation

Familial isolated clinodactyly of finger

Familial isolated congenital asplenia

Familial isolated trichomegaly

Familial magnesium deficiency

Familial multiple lipomatosis

Familial multiple nevi flammei

Familial Ménière disease

Familial nasal acilia

Familial neonatal seizures

Familial neoplastic disease18

Familial non-neuropathic amyloidosis3

Familial non-obstructive reflux-associated chronic pyelonephritis

Familial obesity

Familial osteoarthropathy of the fingers

Familial osteochondritis dissecans

Familial osteodysplasia Anderson type

Familial painful callosities

Familial paroxysmal rhabdomyolysis

Familial patent arterial duct

Familial penile hypospadias

Familial pericarditis

Familial pigmented purpuric eruption

Familial porphyria cutanea tarda

Familial pulmonary capillary hemangiomatosis

Familial recurrent peripheral facial palsy

Familial renal iminoglycinuria

Familial supernumerary nipple

Familial temporal lobe epilepsy

Familial thoracic aortic aneurysm and aortic dissection

Familial thrombomodulin anomalies

Familial vesicoureteral reflux

Haber's syndrome

Heredofamilial systemic amyloidosis affecting skin1

Hyperinsulinism due to insulin receptor deficiency

Idiopathic familial dystonia2

Isolated familial renal hypomagnesemia

Normopepsinogenemic familial duodenal ulcer

Primary generalized glucocorticoid resistance

Retinal arterial macroaneurysm with supravalvular pulmonic stenosis