• Fabry disease

• Facial arteriovenous malformation

• Facial asymmetry

• Facial clefts

• Facial myokymia

• Facial paralysis disorder (TM)

• Facioscapulohumeral form of spinal muscular atrophy

• Facioscapulohumeral form of spinal muscular atrophy with sensory loss

• Facioscapulohumeral muscular dystrophy

• Factitious cheilitis

• Factitious disorder imposed on another

• Factitious disorder imposed on self

• Factitious disorders

• Factitious skin disease

• Factitious skin disorder imposed on another

• Faecal incontinence

• Failed attempted abortion

• Failed induction of labour

• Failed instrumental induction of labour

• Failed medical abortion, complicated by delayed or excessive haemorrhage

• Failed medical abortion, complicated by embolism

• Failed medical abortion, complicated by genital tract or pelvic infection

• Failed medical abortion, with other or unspecified complications

• Failed medical abortion, without complication

• Failed medical induction of labour

• Failed or difficult intubation

• Failed or difficult intubation during pregnancy

• Failure of tooth eruption

• Failure to thrive in infant or child

• Failure to thrive in newborn

• False labour

• False labour before 37 completed weeks of gestation

• Familial abdominal aortic aneurysm

• Familial adenomatous polyposis

• Familial adenomatous polyposis with intestinal malignancy

• Familial amyloid polyneuropathy

• Familial aortic dissection

• Familial apolipoprotein C-II deficiency

• Familial atrial fibrillation

• Familial avascular necrosis of femoral head

• Familial camptodactyly

• Familial capillary haemangioma

• Familial CD8 deficiency

• Familial cerebral saccular aneurysm

• Familial chondromalacia patellae

• Familial cold autoinflammatory syndrome

• Familial cutaneous collagenoma

• Familial defective apolipoprotein B-100

• Familial dementia, British type

• Familial dementia, Danish type

• Familial digital arthropathy - brachydactyly

• Familial dilated cardiomyopathy

• Familial drusen

• Familial exudative vitreoretinopathy

• Familial focal epilepsy with variable foci

• Familial glucocorticoid deficiency

• Familial haemophagocytic lymphohistiocytosis

• Familial hemiplegic migraine

• Familial hyperaldosteronism

• Familial hyperaldosteronism type 1

• Familial hyperaldosteronism type 2

• Familial hyperaldosteronism type 3

• Familial hypercholesterolaemia

• Familial hypercholesterolaemia - heterozygous

• Familial hypercholesterolaemia - homozygous

• Familial hyperlipoproteinaemia type 4

• Familial hyperlipoproteinaemia type 5

• Familial hyperthyroidism

• Familial hypertrophic cardiomyopathy

• Familial hyperuricemic nephropathy

• Familial hypoaldosteronism

• Familial hypobetalipoproteinaemia

• Familial hypocalciuric hypercalcaemia

• Familial hypokalaemia - hypomagnesaemia

• Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis

• Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis - severe ocular involvement

• Familial infantile bilateral striatal necrosis

• Familial infantile myasthenia

• Familial isolated arrhythmogenic right ventricular dysplasia

• Familial isolated dilated cardiomyopathy

• Familial isolated hyperparathyroidism

• Familial isolated hypoparathyroidism

• Familial isolated hypoparathyroidism due to agenesis of parathyroid gland

• Familial isolated hypoparathyroidism due to impaired parathormone secretion

• Familial isolated restrictive cardiomyopathy

• Familial joint laxity

• Familial juvenile hyperuricaemic nephropathy

• Familial lecithin-cholesterol acyltransferase deficiency

• Familial lipoprotein lipase deficiency

• Familial mediterranean fever

• Familial multiple café-au-lait macules

• Familial multiple keratoacanthomas

• Familial multiple lipomata

• Familial multiple system tauopathy

• Familial nonpolyposis colorectal cancer

• Familial osteochondritis dissecans

• Familial pancreatic carcinoma

• Familial papillary renal cell carcinoma

• Familial partial lipodystrophy associated with PLIN1 mutations

• Familial partial lipodystrophy associated with PPARG mutations

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