Disease Index - fa

Fabry Disease
Fabry Disease, Cardiac Variant
Fabry's Disease
Face blindness
Face Pain
Facial Asymmetries
Facial Asymmetry
Facial clefting syndrome, Gypsy type
Facial Dermatoses
Facial Dermatosis
Facial Diplegia, Congenital
Facial Dysplasia, Lateral
Facial Dysplasias, Lateral
Facial Ectodermal Dysplasia
Facial Ectodermal Dysplasias
Facial Hemiatrophies
Facial Hemiatrophies, Progressive
Facial Hemiatrophy
Facial Hemiatrophy of Romberg
Facial Hemiatrophy, Progressive
Facial Hypertrichosis
Facial Injuries
Facial Injury
Facial Myokymia
Facial Myokymias
Facial Neoplasm
Facial Neoplasms
Facial Nerve Avulsion
Facial Nerve Avulsions
Facial Nerve Disease
Facial Nerve Diseases
Facial Nerve Disorder
Facial Nerve Disorders
Facial Nerve Injuries
Facial Nerve Injury
Facial Nerve Motor Disorders
Facial Nerve Sensory Disorders
Facial Nerve Trauma
Facial Nerve Traumas
Facial Neuralgia
Facial Neuralgias
Facial Neuritides
Facial Neuritis
Facial Neuropathies
Facial Neuropathies, Acquired
Facial Neuropathies, Familial
Facial Neuropathy
Facial Neuropathy, Acquired
Facial Neuropathy, Cheilitis Granulomatosa, Orofacial Edema
Facial Neuropathy, Familial
Facial Neuropathy, Idiopathic Acute
Facial Neuropathy, Inflammatory, Acute
Facial Neuropathy, Orofacial Edema, Cheilitis Granulomatosa
Facial Neuropathy, Traumatic
Facial Pain
Facial Pain Syndrome
Facial Pain Syndromes
Facial Pain, Neuralgic
Facial Pain, Referred
Facial Palsies
Facial Palsy
Facial Palsy, Lower Motor Neuron
Facial Palsy, Partial, With Urinary Abnormalities
Facial Palsy, Upper Motor Neuron
Facial Paralyses, Central
Facial Paralyses, Herpetic
Facial Paralyses, Idiopathic
Facial Paralyses, Peripheral
Facial Paralysis
Facial Paralysis, Central
Facial Paralysis, Herpetic
Facial Paralysis, Idiopathic
Facial Paralysis, Peripheral
Facial Paresis
Facial paresis partial unilateral
Facial Paresis, Partial, Unilateral
Facial Recognition Agnosia
Facial Recognition Agnosias
Facial Spasm, Unilateral
Facial Spasms, Unilateral
Facial-Oral Apraxia
Facial-Oral Apraxias
Facies
Facio-Digito-Genital Dysplasia
Facio-Genito-Popliteal Syndrome
Facio-Labio-Pharyngo-Glosso-Laryngo-Brachial Paralysis
Facio-Oculo-Acoustico-Renal syndrome
Facio-Pharyngo-Glossal Diplegia with Automatic-Voluntary Movement Dissociation
Facio-Scapulo-Humeral Dystrophy
Facio-thoraco-skeletal syndrome
Facioauriculovertebral Dysplasia
Facioauriculovertebral Dysplasias
Facioauriculovertebral Sequence
Facioauriculovertebral Sequences
Faciocutaneoskeletal Syndrome
Faciocutaneoskeletal Syndromes
Faciodigitogenital Syndrome
Faciodigitogenital Syndrome, Recessive
Faciogenital Dysplasia
Faciogenitopopliteal Syndrome
Faciooculoacousticorenal syndrome
Faciopalatoosseous syndrome
Facioscapulohumeral Atrophies
Facioscapulohumeral Atrophy
Facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles
Facioscapulohumeral Muscular Dystrophies
Facioscapulohumeral Muscular Dystrophy
Facioscapulohumeral muscular dystrophy 1a
Facioscapulohumeral Muscular Dystrophy 1B
Facioscapulohumeral muscular dystrophy, infantile
Facioscapulohumeral Type Progressive Muscular Dystrophy
Facioscapuloperoneal Muscular Dystrophy
Faciothoracoskeletal Syndrome
Factitious Disorders
Factor 10 Deficiencies
Factor 10 Deficiency
Factor 11 Deficiencies
Factor 11 Deficiency
Factor 12 Deficiencies
Factor 12 Deficiency
Factor 13 Deficiencies
Factor 13 Deficiency
Factor 5 Deficiencies
Factor 5 Deficiency
Factor 7 Deficiencies
Factor 7 Deficiency
Factor 8 deficiency, acquired
Factor 8 Deficiency, Congenital
Factor D Deficiency
Factor Deficiency, Hageman
Factor Eleven Deficiencies
Factor Eleven Deficiency
Factor Five Deficiencies
Factor Five Deficiency
Factor H Deficiency
Factor II Deficiencies
Factor II Deficiency
Factor IX Deficiencies
Factor IX Deficiency
Factor Seven Deficiencies
Factor Seven Deficiency
Factor Ten Deficiencies
Factor Ten Deficiency
Factor Thirteen Deficiencies
Factor Thirteen Deficiency
Factor Twelve Deficiencies
Factor Twelve Deficiency
Factor V And Factor VIII, Combined Deficiency Of
Factor V And Factor VIII, Combined Deficiency Of, With Normal Protein C And Protein C Inhibitor
Factor V Deficiencies
Factor V Deficiency
Factor V Leiden Thrombophilia
Factor V Quebec
Factor VII Deficiencies
Factor VII Deficiency
Factor VIII Deficiency
Factor VIII deficiency, acquired
Factor VIII Deficiency, Congenital
Factor X Deficiencies
Factor X Deficiency
Factor XI Deficiencies
Factor XI Deficiency
Factor XII Deficiencies
Factor XII Deficiency
Factor XIII Deficiencies
Factor XIII Deficiency
Factors II, VII, IX, And X, Combined Deficiency Of
FAD1
FAE (Fetal Alcohol Effects)
FAEs (Fetal Alcohol Effects)
Fahr's disease
Fahr's syndrome
FAIDS
Failed Back Surgery Syndrome
Failure of Tooth Eruption, Primary
Failure to Thrive
Failure, Acute Hepatic
Failure, Acute Liver
Failure, Acute-On-Chronic Liver
Failure, Acute-On-Chronic Liver (ACLF)
Failure, Bone Marrow
Failure, Chronic Liver
Failure, Circulatory
Failure, Hypercapnic Respiratory
Failure, Hypoxemic Respiratory
Failure, Intestinal
Failure, Kidney
Failure, Multiple Organ
Failure, Progressive Autonomic
Failure, Prosthesis
Failure, Renal
Failure, Respiratory
Failures, Acute-On-Chronic Liver
Failures, Acute-On-Chronic Liver (ACLF)
Failures, Chronic Liver
Failures, Kidney
Failures, Progressive Autonomic
Failures, Prosthesis
Failures, Renal
Faint, Neurally Mediated
Fainting
Faints, Neurally Mediated
Fairbank-Keats syndrome
Faisalabad histiocytosis
Falciparum Malaria
FALDH Deficiency
Fallen Urinary Bladder
Fallopian Tube Cancer
Fallopian Tube Cancers
Fallopian Tube Disease
Fallopian Tube Diseases
Fallopian Tube Neoplasm
Fallopian Tube Neoplasms
Fallot Tetralogy
Fallot Trilogy
Fallot's Tetralogy
Fallot's Trilogy
Fallots Tetralogy
Fallots Trilogy
False Aneurysm
False Aneurysm, Carotid
False Aneurysms
False Bundle-Branch Block Syndrome
FAME1
FAME2
FAME3
Familiaere Cholesterin-Pneumonie
Familial Abdominal 3 Aortic Aneurysm
Familial acanthosis nigricans
Familial Acoustic Neuroma
Familial Acoustic Neuromas
Familial Acute Myeloid Leukaemia
Familial Acute Myeloid Leukemia with Mutated Cebpa
Familial Adenomatous Polyposes
Familial Adenomatous Polyposis
Familial Adenomatous Polyposis Coli
Familial Adenomatous Polyposis of the Colon
Familial Adenomatous Polyposis, Attenuated
Familial Advanced Sleep-Phase Syndrome
Familial Afibrinogenemia
Familial Afibrinogenemias
Familial alpha Lipoprotein Deficiency Disease
Familial alpha-Lipoprotein Deficiency Disease
Familial Alzheimer Disease (FAD)
Familial Alzheimer Diseases (FAD)
Familial Amaurotic Idiocy
Familial amniotic bands
Familial Amyloid Neuropathies
Familial Amyloid Neuropathy
Familial Amyloid Neuropathy, Andrade Type
Familial Amyloid Neuropathy, Finnish Type
Familial Amyloid Neuropathy, Portuguese Type
Familial Amyloid Polyneuropathies
Familial Amyloid Polyneuropathy
Familial Amyloid Polyneuropathy Type Iv
Familial Amyloid Polyneuropathy, Appalachian Type
Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Type I
Familial Amyloid Polyneuropathy, Type II
Familial Amyloid Polyneuropathy, Type III
Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type V
Familial Amyloid Polyneuropathy, Type VI
Familial Amyloidoses
Familial Amyloidosis
Familial Amyloidosis, Finnish Type
Familial Angiolipomatosis
Familial antiphospholipid syndrome
Familial Aortic Aneurysm
Familial Aortic Dissection
Familial aplasia cutis congenita of the scalp
Familial Aplasia of the Vermis
Familial Apple Peel Jejunal Atresia
Familial Ataxia, Friedreich
Familial Ataxia, Friedreich's
Familial Atrial Fibrillation
Familial Atrial Fibrillations
Familial Atypical Mole Malignant Melanoma Syndrome
Familial Atypical Mole-Malignant Melanoma Syndrome
Familial Atypical Multiple Mole Melanoma
Familial Atypical Multiple Mole-Melanoma
Familial Atypical Mycobacterioses
Familial Atypical Mycobacteriosis
Familial auditory neuropathy
Familial auto-immune hemolytic anemia
Familial Azotemia
Familial Benign Chronic Pemphigus
Familial Benign Giant-Cell Tumor of the Jaw
Familial Benign Hypercalcemia 1
Familial benign hypercalcemia type 1
Familial Benign Neonatal Convulsions
Familial Benign Neonatal Epilepsy
Familial Benign Recurrent Vertigo
Familial Brachial Plexus Neuritis
Familial Breast Cancer
Familial Caffey Disease
Familial Caffey's Disease
Familial Caffeys Disease
Familial Cavernous Angioma
Familial Cavernous Angiomas
Familial cavernous hemangioma
Familial Cavernous Malformation
Familial Cavernous Malformations
Familial Cerebello Retinal Angiomatosis
Familial Cerebello-Retinal Angiomatoses
Familial Cerebello-Retinal Angiomatosis
Familial Cerebelloretinal Angiomatoses
Familial Cerebelloretinal Angiomatosis
Familial Cerebral Amyloid Angiopathy
Familial cerebral cavernous angioma
Familial cerebral cavernous malformation
Familial cerebral sarcomas
Familial CHARGE Syndrome
Familial CHARGE Syndromes
Familial chronic mucocutaneous candidiasis
Familial Chylomicronemia
Familial Chylomicronemias
Familial Cirrhosis
Familial Cirrhosis with Pulmonary Hypertension
Familial Cold Autoinflammatory Syndrome
Familial Cold Autoinflammatory Syndrome 1
Familial Cold Autoinflammatory Syndrome 2
Familial Cold Induced Autoinflammatory Syndrome
Familial Cold Urticaria
Familial Cold Urticarias
Familial Cold-Induced Autoinflammatory Syndrome
Familial Combined Hyperlipidemia
Familial Combined Hyperlipidemias
Familial Combined Hyperlipoproteinemia
Familial Combined Hyperlipoproteinemias
Familial congenital heart block
Familial Creutzfeldt Jakob Disease
Familial Creutzfeldt-Jakob Disease
Familial Creutzfeldt-Jakob Diseases
Familial Cutaneous Collagenoma
Familial cyclic vomiting syndrome
Familial cylindromatosis
Familial Cystic Parathyroid Adenomatosis
Familial Dandy-Walker Syndrome
familial Danish Dementia
Familial Danish dementia
Familial Dementia
Familial Dementia with Neuroserpin Inclusion Bodies
Familial Dementias
Familial Dental Ageneses
Familial Dental Agenesis
Familial Dermatofibrosarcoma Protuberan
Familial Dermatofibrosarcoma Protuberans
familial dermatographia
Familial dermatographism
familial dermographic urticaria
Familial dermographism
familial dilated cardiomyopathy
Familial duodenal atresia
Familial Dysalbuminemic Hyperthyroxinemia
Familial Dysautonomia
Familial Dysautonomia, Type 2
Familial Dysautonomia, Type II
Familial Dysbetalipoproteinemia
Familial Dyskeratotic Comedones
Familial Dyskinesia with Facial Myokymia
Familial Dystonia
Familial Dystonia, Autosomal Dominant
Familial Dystonia, Autosomal Recessive
Familial Dystonia, Idiopathic
Familial Dystonias
Familial Dystonias, Idiopathic
Familial Ebstein Anomaly
Familial Ebstein's Anomaly
Familial Ebsteins Anomaly
Familial ectopia lentis
Familial ectopic pupil
Familial encephalopathy with neuroserpin inclusion bodies
Familial Endocrine Adenomatoses
Familial Endocrine Adenomatosis
Familial Eosinophilia
Familial eosinophilia
Familial ependymoma
Familial Epilepsies
Familial Epilepsy
Familial Erythrocytosis
Familial erythrocytosis, 1
Familial Erythromelalgia
Familial Erythrophagocytic Lymphohistiocytoses
Familial Erythrophagocytic Lymphohistiocytosis
Familial Exostoses
Familial Exostosis
Familial expansile osteolysis
Familial Extrahepatic Biliary Atresia
Familial Exudative Vitreoretinopathies
Familial Exudative Vitreoretinopathy
Familial Facial Neuropathies
Familial Facial Neuropathy
Familial Fat Induced Hypertriglyceridemia
Familial Fat-Induced Hypertriglyceridemia
Familial Fat-Induced Hypertriglyceridemias
Familial Fatal Epstein Barr Infection
Familial Fatal Epstein-Barr Infection
Familial Fatal Insomnia
Familial Fatal Insomnias
Familial Fatal, Insomnia
Familial Fatals, Insomnia
Familial Felty Syndrome
Familial Felty's Syndrome
Familial Feltys Syndrome
Familial Fibrous Dysplasia of Jaw
Familial Form of Canavan Disease
Familial foveal retinoschisis
Familial Gestational Hyperthyroidism
Familial Gigantiform Cementoma
Familial Glucocorticoid Deficiency 1
Familial Glucocorticoid Deficiency 2
Familial Gonadotrophin-Independent Sexual Precocity
Familial Gout-Kidney Disease
Familial Gouty Nephropathy
Familial Granulomatosis, Blau Type
Familial Guillain-Barre Syndrome
Familial Guillain-Barre Syndromes
Familial Gynecomastia
Familial Hemifacial Spasm
Familial Hemiplegic Migraine
Familial hemiplegic migraine, type 2
Familial Hemiplegic Migraines
Familial Hemochromatoses
Familial Hemochromatosis
Familial Hemophagocytic Histiocytoses
Familial Hemophagocytic Histiocytosis
Familial Hemophagocytic Lymphocytoses
Familial Hemophagocytic Lymphocytosis
Familial Hemophagocytic Lymphohistiocytoses
Familial Hemophagocytic Lymphohistiocytosis
Familial Hemophagocytic Reticuloses
Familial Hemophagocytic Reticulosis
Familial Hibernation (Kleine-Levin) Syndrome
Familial Hibernian fever
familial Hidradenitis suppurativa
Familial High Density Lipoprotein Deficiency Disease
Familial High-Density Lipoprotein Deficiency Disease
Familial Histiocytic Reticuloses
Familial Histiocytic Reticulosis
familial horizontal gaze palsy with progressive scoliosis
Familial Horizontal Gaze Palsy with Progressive Scoliosis
Familial Hyperaldosteronism
Familial Hypercalciuric Hypocalcemia
Familial Hypercholesterolemia
Familial Hypercholesterolemia with Hyperlipemia
Familial Hypercholesterolemias
Familial Hypercholesterolemic Xanthomatoses
Familial Hypercholesterolemic Xanthomatosis
Familial Hyperchylomicronemia
Familial hyperchylomicronemia syndrome
Familial Hyperchylomicronemias
Familial Hyperekplexia
Familial Hyperekplexias
Familial Hyperinsulinemic Hypoglycemia 1
Familial Hyperinsulinism
Familial Hyperinsulinisms
Familial Hyperkalemic Periodic Paralysis
Familial Hyperlipemia, Essential
Familial Hyperlipemias, Essential
Familial Hyperlipoproteinemia Type 1
Familial Hyperlipoproteinemia Type 4
Familial Hyperlysinemia
Familial Hyperlysinemias
Familial Hyperphosphatemic Tumoral Calcinosis
Familial Hyperpotassemia and Hypertension
Familial Hypertensive Hyperkalemia
Familial Hypertensive Hyperkalemias
Familial Hypertriglyceridemia
Familial Hypertrophic Cardiomyopathies
Familial Hypertrophic Cardiomyopathy
Familial Hypertryptophanemia
Familial Hypo-RBP
Familial Hypoadrenocorticism
Familial Hypoadrenocorticisms
Familial Hypoalphalipoproteinemia
Familial Hypoalphalipoproteinemias
Familial Hypobetalipoproteinemia
Familial hypocalciuric hypercalcemia
Familial Hypokalemia Hypomagnesemia
Familial Hypokalemia-Hypomagnesemia
Familial Hypokalemic Periodic Paralysis
Familial hypomagnesemia - hypercalciuria
Familial Hypophosphatemia
Familial Hypophosphatemias
Familial Hypophosphatemic Rickets
Familial hypotransferrinemia
Familial idiopathic basal ganglia calcification
Familial Idiopathic Cardiomyopathies
Familial Idiopathic Cardiomyopathy
Familial Idiopathic Hyperphosphatasemia
familial Idiopathic inflammatory myopathy
Familial Idiopathic Osteoarthropathy Of Childhood
Familial Idiopathic Pulmonary Fibrosis
Familial Idiopathic Scoliosis Associated with Congenital Encephalopathy
Familial Incomplete Male Pseudohermaphroditism, Type 2
familial Infantile convulsions and paroxysmal choreoathetosis
Familial Infantile Cortical Hyperostosis
Familial Infantile Encephalopathy with Intracranial Calcification and Chronic Cerebrospinal Fluid Lymphocytosis
Familial Infantile Scoliosis Associated with Bilateral Paralysis of Conjugate Gaze
Familial infiltrative fibromatosis
Familial Intestinal Polyatresia Syndrome
Familial Intestinal Polyposes
Familial Intestinal Polyposis
Familial intrahepatic cholestasis of pregnancy
Familial islet cell tumors
Familial isolated deficiency of vitamin E
Familial Isolated Pituitary Adenoma
Familial Isolated Vitamin E Deficiency
Familial joint instability syndrome
familial Joint laxity
Familial Juvenile 2 Hyperuricemic Nephropathy
Familial Juvenile Hyperuricemic Nephropathy
Familial Juvenile Hyperuricemic Nephropathy 2
familial juvenile Nephronophthisis
Familial Juvenile Parkinsonism
Familial Juvenile Systemic Granulomatosis
Familial Kleine Levin Syndrome
Familial Kleine-Levin Syndrome
Familial Lichen Planus
Familial Lipochrome Histiocytosis
Familial lipomyelomeningocele
Familial Lipoprotein Lipase Deficiency
Familial LPL Deficiencies
Familial LPL Deficiency
Familial Male-Limited Precocious Puberty
familial Marcus Gunn phenomenon
Familial Mediterranean Fever
Familial Mediterranean Fever, Autosomal Dominant
Familial Mediterranean Fever, Autosomal Recessive
Familial medullary thyroid carcinoma
Familial Melanoma
Familial Melanomas
familial Meningioma
Familial meningioma
Familial mesangial sclerosis
Familial Mesial Temporal Lobe Epilepsy
Familial Metabolic Brain Diseases
Familial Metabolic Disorders, Brain
Familial Mixed Cryoglobulinemia
Familial Motor Neuron Disease
Familial Multilocular Cystic Disease of the Jaws
Familial Multiple Coagulation Factor Deficiency I
Familial Multiple Coagulation Factor Deficiency III
Familial Multiple Lipoma
Familial Multiple Lipomas
Familial Multiple Lipomatoses
Familial Multiple Lipomatosis
Familial Multiple Polyposes
Familial Multiple Polyposi
Familial Multiple Polyposis
Familial Multiple Polyposis Syndrome
Familial Multiple Polyposus
Familial Nephritis
Familial Nodular Heterotopia
Familial Nodular Heterotopias
Familial Non Immune Hydrops Fetalis
Familial Non-Immune Hydrops Fetalis
Familial Nonhemolytic Jaundice
Familial Nonhemolytic Unconjugated Hyperbilirubinemia
Familial Nonmedullary Thyroid Cancer
Familial Nonpolyposis Colon Cancer
Familial Nonpolyposis Colon Cancer Type 1
familial Nuchal bleb
Familial nuchal bleb
Familial Olivopontocerebellar Atrophies
Familial Olivopontocerebellar Atrophy
Familial Osteochondritis Dissecans
Familial Osteoectasia
Familial oto-facio-cervical dysmorphia
Familial Paget's disease of bone
Familial Pancreatitis
Familial Parkinson Disease, Autosomal Recessive
Familial paroxysmal choreoathetosis
Familial paroxysmal dystonia
Familial Paroxysmal Kinesigenic Dyskinesia
Familial Paroxysmal Nonkinesigenic Dyskinesia
Familial Paroxysmal Polyserositides
Familial Paroxysmal Polyserositis
Familial Partial Lipodystrophies
Familial Partial Lipodystrophy
Familial Partial Lipodystrophy, Kobberling Type
Familial Partial Lipodystrophy, Type 1
Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 3
familial Pemphigus vulgaris
Familial pemphigus vulgaris
Familial Pemphigus, Benign
Familial Perifolliculitis Capitis Abscedens Et Suffodiens
Familial Periodic Paralyses
Familial Periodic Paralysis
Familial Persistent Pulmonary Hypertension of the Newborn
Familial pheochromocytoma
Familial Pick Disease
Familial Pick's Disease
Familial Pick's Diseases
Familial Picks Disease
Familial pigmented purpuric eruption
Familial pityriasis rubra pilaris
Familial Plantar Fibromatosis
Familial Platelet Disorder with Associated Myeloid Malignancy
Familial Platelet Storage Pool Disease
Familial Polycythemia
Familial polymorphic ventricular tachycardia
Familial Polyneuropathies
Familial Polyneuropathy
Familial Polyposis Coli
Familial Polyposis Colus
Familial Polyposis of the Colon
Familial Polyposis Syndrome
Familial Polyposis Syndromes
Familial Polythelia
Familial Porencephalic White Matter Disease
Familial Porencephaly
Familial Portuguese Polyneuritic Amyloidosis
Familial Precocious Puberties
Familial Precocious Puberty
familial Premature ovarian failure
Familial premature ovarian failure
Familial Pressure Sensitive Neuropathy
Familial primary biliary cirrhosis
Familial primary gastric lymphoma
Familial Primary Hyperparathyroidism with Multiple Ossifying Jaw Fibromas
Familial Primary Pulmonary Hypertension
Familial Progressive Hyperpigmentation
Familial Progressive Myoclonic Epilepsy
Familial progressive supranuclear palsy
familial Prostate cancer
Familial Pterygium Syndrome
Familial Pyrimidemia
Familial Pyrimidemias
Familial Pyrimidinemia
Familial Pyrimidinemias
Familial Rectal Pain
Familial recurrent arthritis
Familial recurrent intrahepatic cholestasis of pregnancy
Familial renal carcinoma
Familial renal cell carcinoma
Familial Restrictive Cardiomyopathy
Familial reticulate acropigmentation of Dohi
Familial Reticuloendothelioses
Familial Reticuloendotheliosis
Familial Retinoblastoma
Familial Retinoblastomas
Familial Schamberg's disease
Familial spasmodic torticollis
Familial Spastic Paraparesis, Htlv 1 Associated
Familial Spastic Paraparesis, Htlv-1-Associated
Familial spastic paraplegia, autosomal dominant 3
Familial spastic paraplegia, autosomal dominant, 1
Familial Spastic Paraplegia, Autosomal Dominant, 3
Familial spinal arachnoiditis
Familial Spinal Neurofibromatosis
Familial Spinocerebellar Degeneration
Familial Spinocerebellar Degenerations
Familial spondyloepiphyseal dysplasia
Familial Sudden Death
Familial Taad
familial Temporal epilepsy
Familial temporal lobe epilepsy
Familial Testotoxicosis
Familial Third and Fourth Pharyngeal Pouch Syndrome
Familial Thoracic 1 Aortic Aneurysm
Familial Thoracic Aortic Aneurysm
Familial Thoracic Aortic Aneurysm and Dissection
Familial Thrombotic Microangiopathy
Familial Thrombotic Thrombocytopenia Purpura
Familial Thrombotic Thrombocytopenic Purpura
Familial Thymoma
Familial thyroglossal duct cyst
Familial Tonic Clonic Epilepsy
Familial Tonic-Clonic Epilepsies
Familial Tonic-Clonic Epilepsy
Familial Tooth Ageneses
Familial Tooth Agenesis
Familial torticollis
Familial transient erythroblastopenia of childhood
Familial Transthyretin Cardiac Amyloidosis
Familial Tremor
Familial Tremors
Familial Trichoepithelioma
Familial True Hermaphroditism
Familial True Hermaphroditisms
Familial Turner Syndrome
Familial tylosis
familial type 2 Hemiplegic migraine
Familial Type IV Hyperlipoproteinemia
Familial Veno-Occlusive Disease with Immunodeficiency
Familial Ventricular Hypertrophies
Familial Ventricular Hypertrophy
Familial Vestibulopathies
Familial Vestibulopathy
familial visceral Amyloidosis
Familial vocal cord dysfunction
Familial Waldenstrom Macroglobulinaemia
Familial Waldenstrom's Macroglobulinaemia
Familial Waldenstroms Macroglobulinaemia
Familial Waldmann's disease
Familial Wilms Tumor 1
Familial X linked Addison Disease
Familial X-linked Addison Disease
Familial Xanthomatoses
Familial Xanthomatosis
Familial XX True Hermaphroditism
Familial Young-Adult-Onset Arteriosclerotic Leukoencephalopathy with Alopecia and Lumbago without Arterial Hypertension
FAMMM Syndrome
FAMMM Syndromes
FANCD1
Fanconi Anemia
Fanconi Anemia, Complementation Group B
Fanconi Anemia, Complementation Group D1
Fanconi Anemia, Complementation Group I
Fanconi Anemia, Complementation Group J
Fanconi Anemias
Fanconi Bickel Syndrome
Fanconi Hypoplastic Anemia
Fanconi like syndrome
Fanconi Pancytopenia
Fanconi Pancytopenia, Type 2
Fanconi Panmyelopathy
Fanconi Renotubular Syndrome
Fanconi Syndrome
Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
Fanconi Syndrome without Cystinosis
Fanconi Syndrome, Adult
Fanconi Syndrome, Renal
Fanconi Type Glycogenosis
Fanconi's Anemia
Fanconi-Bickel Syndrome
Fanconi-Bickel Syndromes
Fanconi-Like Syndrome
Far East Scarlet like Fever
Far East Scarlet-like Fever
Far Eastern Russian Encephalitis
Far Eastern Spotted Fever
Fara Chlupackova syndrome
Farabee-Type Brachydactyly
Farber Disease
Farber Lipogranulomatosis
Farber's Disease
Farber's Diseases
Farbers Disease
Farmer Lung
Farmer's Lung
Farmer's Lungs
Farmers Lung
Farsightedness
Fascial Dystrophy, Congenital
Fascicular Block
Fascicular Block, Anterior
Fascicular Block, Posterior
Fascicular Blocks
Fascicular Blocks, Anterior
Fascicular Blocks, Posterior
Fasciculation
Fasciculation Cramp Syndrome, Benign
Fasciculation, Benign
Fasciculation, Muscular
Fasciculation, Skeletal Muscle
Fasciculation, Tongue
Fasciculation-Cramp Syndrome, Benign
Fasciculation-Cramp Syndromes, Benign
Fasciculations
Fasciculations, Benign
Fasciculations, Muscular
Fasciculations, Skeletal Muscle
Fasciculations, Tongue
Fasciculoventricular Accessory Pathway
Fasciculoventricular Accessory Pathways
Fasciculoventricular Pathway
Fasciculoventricular Pathways
Fasciitides
Fasciitides, Necrotizing
Fasciitis
Fasciitis, Chronic Plantar
Fasciitis, Necrotizing
Fasciitis, Plantar
Fasciitis, Plantar, Chronic
Fasciola Infection
Fasciola Infections
Fascioliases
Fascioliasis
Fascioloidiases
Fascioloidiasis
Fasciolopsiases
Fasciolopsiasis
Fascitides
Fascitides, Necrotizing
Fascitis
Fascitis, Necrotizing
FASD
FASDs
Fasps
Fast-Channel Congenital Myasthenic Syndrome
Fasting Hypoglycemia
Fat Embolism
Fat Embolism Syndrome
Fat Embolisms
Fat Necroses
Fat Necrosis
Fat Necrosis, Peripancreatic
Fat-Induced Hypertriglyceridemia, Familial
Fat-Induced Hypertriglyceridemias, Familial
Fatal Familial Insomnia
Fatal Familial Insomnias
Fatal Infantile Lactic Acidosis
Fatal Insomnia, Familial
Fatal Insomnias, Familial
Fatal neonatal hepatic steatosis
Fatal, Insomnia Familial
Fatals, Insomnia Familial
Fatigable Positional Nystagmus
Fatigue
Fatigue Disorder, Chronic
Fatigue Fracture
Fatigue Fractures
Fatigue Syndrome, Chronic
Fatigue Syndrome, Postviral
Fatigue Syndromes, Chronic
Fatigue, Alarm
Fatigue, Compassion
Fatigue, Emotional
Fatigue, Eye
Fatigue, Heat
Fatigue, Mental
Fatigue, Visual
Fatigue, Voice
Fatigue-Fibromyalgia Syndrome, Chronic
Fatigue-Fibromyalgia Syndromes, Chronic
Fatigues, Voice
Fatty Acid Hydroxylase-Associated Neurodegeneration
Fatty Alcohol:NAD+ Oxidoreductase Deficiency
Fatty Aldehyde Dehydrogenase Deficiency
Fatty Aldehyde Dehydrogenase Deficiency Disease
Fatty Liver
Fatty Liver Disease, Congenital
Fatty Liver with Encephalopathy
Fatty Liver, Alcoholic
Fatty Liver, Nonalcoholic
Fatty Livers, Nonalcoholic
Fatty Streak, Arterial
Fatty Tumor
Fatty Tumors
FATWO Female adnexal tumor of probable Wolffian origin
Favism
Favisms
Favre Hyaloideoretinal Degeneration
Favre Racouchot Syndrome
Favre-Racouchot Syndrome
Favus
Fazio Londe Disease
Fazio Londe Syndrome
Fazio Londe's Disease
Fazio Londe's Syndrome
Fazio-Londe Disease
Fazio-Londe Syndrome
Fazio-Londe's Disease
Fazio-Londe's Syndrome