Toggle navigation
MedBind ICD 10
ICD 10 Codes
ICD 10 Code Indexes
ICD 10 Procedure Codes
Health Topic
ICD 10 Code Definition
Close
Search
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
1
2
3
4
5
6
Next »
Advertise