Encyclopedia of Molecular Mechanisms of Disease

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Biomedical and Life Sciences > Encyclopedia of Molecular Mechanisms of Disease

Encyclopedia of Molecular Mechanisms of Disease

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Fabry Disease Facial Paralysis Facioscapulohumeral Disease → Facioscapulohumeral Muscular Dystrophy Facioscapulohumeral Muscular Dystrophy Factor IX Deficiency → Hemophilia B Factor V Leiden → Thrombosis, Venous Factor V Leiden, Resistance against Activated Protein C Factor VIII Deficiency → Hemophilia A Factor XI Deficiency → Hemophilia C FAH Deficiency Fairbank Type Dysplasia → Multiple Epiphyseal Dysplasia FAME → Epilepsies, Familial Benign Myoclonic Familial Adenomatous Polyposis → Adenomatous Polyposis, Familial Familial Adult Myoclonic Epilepsy → Epilepsies, Familial Benign Myoclonic Familial Anterior Hypopituitarism → Hypopituitarism Familial Benign Chronic Pemphigus → Hailey-Hailey Disease Familial Benign Hypercalcemia → Hypercalcemia, Familial Hypocalciuric Familial Benign Hypocalciuric Hypercalcemia → Hypercalcemia, Familial Hypocalciuric Familial Benign Myoclonic Epilepsies → Epilepsies, Familial Benign Myoclonic Familial Benign Myoclonus Epilepsy with Adult Onset → Epilepsies, Familial Benign Myoclonic Familial CD8 Deficiency → CD8 Deficiency Familial Chloride Diarrhea → Chloride Diarrhea, Congenital Familial Combined Hyperlipidemia → Hyperlipidemia, Combined Familial Cortical Myoclonic Tremor → Epilepsies, Familial Benign Myoclonic Familial Cortical Myoclonic Tremor with Epilepsy → Epilepsies, Familial Benign Myoclonic Familial Cortical Tremor with Epilepsy → Epilepsies, Familial Benign Myoclonic Familial Cylindromatosis → Cylindromatosis, Familial Familial Defective ApoB-100 → Ligand-defective Apolipoprotein B-100, Familial Familial Dysautonomia → Catecholamine Deficiency Familial Dysbetalipoproteinemia → Dysbetalipoproteinemia, Familial Familial Dysproteinemia → Intestinal Lymphangiectasia Familial Essential Myoclonus and Epilepsy → Epilepsies, Familial Benign Myoclonic Familial Hematuria → Hematuria Familial Hemiplegic Migraine → Migraine, Familial Hemiplegic Familial HUS → Hemolytic Uremic Syndrome Familial Hypercalciuric Hypocalcaemia Familial Hypercholanemia → Cholestasis, Progressive Familial Intrahepatic Familial Hypercholesterolemia → Hypercholesterolemia, Familial Familial Hyperinsulinism → Persistent Hyperinsulinemic Hypoglycemia Familial Hypoalphalipoproteinemia → Tangier Disease Familial Hypobetalipoproteinemia Familial Hypocalcemia → Hypoparathyroidism, Familial	Familial Hypocalciuric Hypercalcemia Familial Hypomagnesemia → Hypomagnesemia Familial Hypoparathyroidism → Hypoparathyroidism, Familial Familial Hypoproteinemia with Lymphangiectatic Enteropathy → Intestinal Lymphangiectasia Familial Incomplete Male Pseudohermaphroditism Type I → Reifenstein Syndrome Familial Isolated Deficiency of Vitamin E → Ataxia due to Vitamin E Deficiency Familial Juvenile Gout → Nephropathy, Familial Juvenile Hyperuricemic Familial Juvenile Hyperuricemic Nephropathy Familial Ligand-defective Apolipoprotein B-100 → Ligand-defective Apolipoprotein B-100, Familial Familial Lipoprotein Lipase Deficiency → Lipoprotein Lipase Deficiency, Familial Familial Mediterranean Fever → Mediterranean Fever, Familial Familial Nonhemolytic Conjugated Hyperbilirubinemia with Normal Liver Histology → Rotor Syndrome Familial Orthostatic Hypotensive Disorder, Streeten Type Familial Paroxysmal Polyserositis → Mediterranean Fever, Familial Familial Periodic Ataxia → Episodic Ataxia Type 1 and Type 2 Familial Periodic Paralyses → Periodic Paralyses, Familial Familial Polymorphic Ventricular Tachycardia → Tachycardia, Polymorphic Ventricular, Stress-induced Familial Protein Intolerance → Lysinuric Protein Intolerance Familial Pulmonary Arterial Hypertension Familial Renal Glucosuria → Glucosuria, Primary Renal Familial Spastic Paraplegia → Spastic Paraplegia, Hereditary Familial Startle Disease → Hyperekplexia, Hereditary Familial Tremor → Tremor, Essential Fanconi Anemia Fanconi Renotubular Syndrome → Fanconi Syndrome Fanconi Syndrome FAP Farabee Type Brachydactyly → Brachydactyly Type A Farber Lipogranulomatosis → Farber's Disease Farber's Disease Farmer's Lung Disease → Hypersensitivity Pneumonitis Farsightedness → Hypermetropia Fasciitis, Eosinophilic Fasciitis, Necrotizing Fat Malabsorption → Steatorrhea Fat Necrosis Fatigue Syndrome → Chronic Fatigue Syndrome Fatty Liver Disease, Nonalcoholic Fatty Liver/Fatty Liver Disease → Hepatic Steatosis Favism → Glucose-6-Phosphate Dehydrogenase Deficiency
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Fabry Disease
Facial Paralysis
Facioscapulohumeral Disease → Facioscapulohumeral Muscular Dystrophy
Facioscapulohumeral Muscular Dystrophy
Factor IX Deficiency → Hemophilia B
Factor V Leiden → Thrombosis, Venous Factor V Leiden, Resistance against Activated Protein C
Factor VIII Deficiency → Hemophilia A
Factor XI Deficiency → Hemophilia C
FAH Deficiency
Fairbank Type Dysplasia → Multiple Epiphyseal Dysplasia
FAME → Epilepsies, Familial Benign Myoclonic
Familial Adenomatous Polyposis → Adenomatous Polyposis, Familial
Familial Adult Myoclonic Epilepsy → Epilepsies, Familial Benign Myoclonic
Familial Anterior Hypopituitarism → Hypopituitarism
Familial Benign Chronic Pemphigus → Hailey-Hailey Disease
Familial Benign Hypercalcemia → Hypercalcemia, Familial Hypocalciuric
Familial Benign Hypocalciuric Hypercalcemia → Hypercalcemia, Familial Hypocalciuric
Familial Benign Myoclonic Epilepsies → Epilepsies, Familial Benign Myoclonic
Familial Benign Myoclonus Epilepsy with Adult Onset → Epilepsies, Familial Benign Myoclonic
Familial CD8 Deficiency → CD8 Deficiency
Familial Chloride Diarrhea → Chloride Diarrhea, Congenital
Familial Combined Hyperlipidemia → Hyperlipidemia, Combined
Familial Cortical Myoclonic Tremor → Epilepsies, Familial Benign Myoclonic
Familial Cortical Myoclonic Tremor with Epilepsy → Epilepsies, Familial Benign Myoclonic
Familial Cortical Tremor with Epilepsy → Epilepsies, Familial Benign Myoclonic
Familial Cylindromatosis → Cylindromatosis, Familial
Familial Defective ApoB-100 → Ligand-defective Apolipoprotein B-100, Familial
Familial Dysautonomia → Catecholamine Deficiency
Familial Dysbetalipoproteinemia → Dysbetalipoproteinemia, Familial
Familial Dysproteinemia → Intestinal Lymphangiectasia
Familial Essential Myoclonus and Epilepsy → Epilepsies, Familial Benign Myoclonic
Familial Hematuria → Hematuria
Familial Hemiplegic Migraine → Migraine, Familial Hemiplegic
Familial HUS → Hemolytic Uremic Syndrome
Familial Hypercalciuric Hypocalcaemia
Familial Hypercholanemia → Cholestasis, Progressive Familial Intrahepatic
Familial Hypercholesterolemia → Hypercholesterolemia, Familial
Familial Hyperinsulinism → Persistent Hyperinsulinemic Hypoglycemia
Familial Hypoalphalipoproteinemia → Tangier Disease
Familial Hypobetalipoproteinemia
Familial Hypocalcemia → Hypoparathyroidism, Familial

Familial Hypocalciuric Hypercalcemia
Familial Hypomagnesemia → Hypomagnesemia
Familial Hypoparathyroidism → Hypoparathyroidism, Familial
Familial Hypoproteinemia with Lymphangiectatic Enteropathy → Intestinal Lymphangiectasia
Familial Incomplete Male Pseudohermaphroditism Type I → Reifenstein Syndrome
Familial Isolated Deficiency of Vitamin E → Ataxia due to Vitamin E Deficiency
Familial Juvenile Gout → Nephropathy, Familial Juvenile Hyperuricemic
Familial Juvenile Hyperuricemic Nephropathy
Familial Ligand-defective Apolipoprotein B-100 → Ligand-defective Apolipoprotein B-100, Familial
Familial Lipoprotein Lipase Deficiency → Lipoprotein Lipase Deficiency, Familial
Familial Mediterranean Fever → Mediterranean Fever, Familial
Familial Nonhemolytic Conjugated Hyperbilirubinemia with Normal Liver Histology → Rotor Syndrome
Familial Orthostatic Hypotensive Disorder, Streeten Type
Familial Paroxysmal Polyserositis → Mediterranean Fever, Familial
Familial Periodic Ataxia → Episodic Ataxia Type 1 and Type 2
Familial Periodic Paralyses → Periodic Paralyses, Familial
Familial Polymorphic Ventricular Tachycardia → Tachycardia, Polymorphic Ventricular, Stress-induced
Familial Protein Intolerance → Lysinuric Protein Intolerance
Familial Pulmonary Arterial Hypertension
Familial Renal Glucosuria → Glucosuria, Primary Renal
Familial Spastic Paraplegia → Spastic Paraplegia, Hereditary
Familial Startle Disease → Hyperekplexia, Hereditary
Familial Tremor → Tremor, Essential
Fanconi Anemia
Fanconi Renotubular Syndrome → Fanconi Syndrome
Fanconi Syndrome
FAP
Farabee Type Brachydactyly → Brachydactyly Type A
Farber Lipogranulomatosis → Farber's Disease
Farber's Disease
Farmer's Lung Disease → Hypersensitivity Pneumonitis
Farsightedness → Hypermetropia
Fasciitis, Eosinophilic
Fasciitis, Necrotizing
Fat Malabsorption → Steatorrhea
Fat Necrosis
Fatigue Syndrome → Chronic Fatigue Syndrome
Fatty Liver Disease, Nonalcoholic
Fatty Liver/Fatty Liver Disease → Hepatic Steatosis
Favism → Glucose-6-Phosphate Dehydrogenase Deficiency

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