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Psychology and Mental Health Dictionary Definitions - Letter F - Psychforums.com





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F


Fabry Disease : Fabry Disease is categorized as a rare disease. Fabry Disease is a ...
facio-genito-popliteal syndrome : See Popliteal Pterygium Syndrome.
Faciodigitogenital Syndrome : See Aarskog-Scott Syndrome.
Faciogenital Dysplasia : See Aarskog-Scott Syndrome.
Facioscapulohumeral Muscular Dystrophy : Facioscapulohumeral Muscular Dystrophy is ...
Factitious disorder : Factitious disorders are conditions in which a person acts as...
Factor II deficiency : Factor II deficiency is categorized as a rare disease. Facto...
Factor V Deficiency : Factor V Deficiency is categorized as a rare disease. Factor ...
Factor V Leiden : See Thrombophilia.
Factor VII deficiency : Factor VII deficiency is categorized as a rare disease. Fac...
Fairbank type Epiphyseal dysplasia : See Multiple Epiphyseal Dysplasia.
Fairbanks disease : See Multiple Epiphyseal Dysplasia.
fallot tetralogy : See Tetralogy of Fallot.
Familial : See Dilated Cardiomyopathy.
Familial adenomatous polyposis : Familial adenomatous polyposis is categorized as a...
Familial Alzheimer Disease : Familial Alzheimer Disease is categorized as a rare di...
Familial Alzheimer´s disease : See Familial Alzheimer Disease.
Familial Alzheimers disease : See Familial Alzheimer Disease.
Familial Breast Cancer : Familial Breast Cancer is categorized as a rare disease. F...
Familial Cold Autoinflammatory Syndrome : Familial Cold Autoinflammatory Syndrome i...
Familial Cold Urticaria : Familial Cold Urticaria is categorized as a rare disease....
Familial Cylindromatosis : See Cylindromatosis.
Familial dysbetalipoproteinemia : See Hyperlipidemia Type 3.
Familial Exudative Vitreoretinopathy : Familial Exudative Vitreoretinopathy is cate...
Familial Hemiplegic Migraine : Familial Hemiplegic Migraine is categorized as a rar...
Familial Hemophagocytic Lymphohistiocytosis : See Hemophagocytic Lymphohistiocytosi...
Familial Hibernian Fever : See TNF Receptor Associated Periodic Syndrome.
Familial Hibernian Syndrome : See TNF Receptor Associated Periodic Syndrome.
Familial hyperchylomicronemia : See Hyperlipoproteinemia type 1.
familial hypogonadism with anosmia : See Kallmann Syndrome.
familial iminoglycinuria : See Iminoglycinuria.
Familial Metaphyseal Dysplasia : See Metaphyseal Dysplasia.
Familial Partial Lipodystrophy : See Lipodystrophy.
familial PKD : See Paroxysmal Kinesigenic Dyskinesia.
Familial Restrictive Cardiomyopathy : See Restrictive Cardiomyopathy.
Familial venous malformations : Familial venous malformations is categorized as a r...
Familial visceral amyloidosis : See Amyloidosis.
Fanconi Anaemia : See Fanconi Anemia.
Fanconi Anemia : Fanconi Anemia is categorized as a rare disease. Fanconi Anemia is...
Fanconi Syndrome : Fanconi Syndrome is categorized as a rare disease. Fanconi Syndr...
Fanconi´s syndrome : See Fanconi Syndrome.
Favism : See Glucose-6-Phosphate Dehydrogenase Deficiency.
FCAS : See Familial Cold Autoinflammatory Syndrome.
FCMD : See Fukuyama Congenital Muscular Dystrophy.
FCU : See Familial Cold Autoinflammatory Syndrome.
febre maculosa : See Rocky Mountain Spotted Fever.
Fellman syndrome : See GRACILE Syndrome.
Femur fibula ulna syndrome : See Femur-Fibula-Ulna Complex.
Femur-Fibula-Ulna Complex : Femur-Fibula-Ulna Complex is categorized as a rare dise...
Fetal cytomegalovirus syndrome : Fetal cytomegalovirus syndrome is categorized as a...
FEVR : See Familial Exudative Vitreoretinopathy.
FFU Complex : See Femur-Fibula-Ulna Complex.
FG Syndrome : FG Syndrome is categorized as a rare disease. FG syndrome is a rare g...
FGFR3-related craniosynostosis : See Muenke Syndrome.
FGS : See FG Syndrome.
FHL : See Hemophagocytic Lymphohistiocytosis.
FHM : See Familial Hemiplegic Migraine.
Fibrinoid degeneration of astrocytes : See Alexander disease.
Fibrinoid leukodystrophy : See Alexander disease.
Fibro : See Fibromyalgia.
Fibrodysplasia Ossificans Progressiva : Fibrodysplasia Ossificans Progressiva is ca...
Fibromuscular Dysplasia : Fibromuscular Dysplasia is categorized as a rare disease....
Fibromuscular Dysplasia of Arteries : See Fibromuscular Dysplasia.
Fibromyalgia : Fibromyalgia is categorized as a rare disease. Fibromyalgia is a dis...
Fibrous dysplasia of bone : Fibrous dysplasia of bone is categorized as a rare dise...
fiebre manchada : See Rocky Mountain Spotted Fever.
Finnish lactic acidosis with hepatic hemosiderosis : See GRACILE Syndrome.
Finnish lethal neonatal metabolic syndrome : See GRACILE Syndrome.
Finnish type amyloidosis : See Amyloidosis.
Fish Malodor Syndrome : See Trimethylaminuria.
Fish Odor Syndrome : See Trimethylaminuria.
fièvre boutonneuse : See Boutonneuse Fever.
FLNMS : See GRACILE Syndrome.
FMD : See Fibromuscular Dysplasia.
FMS : See Fibromyalgia.
Focal Dystonia : Focal Dystonia is categorized as a rare disease. Focal Dystonia is...
Focal epilepsy : See Temporal Lobe Epilepsy.
Follicular Lymphoma : Follicular Lymphoma is categorized as a rare disease. If you ...
Fong Disease : See Nail-Patella Syndrome.
foodborne botulism : See Botulism.
FOP : See Fibrodysplasia Ossificans Progressiva.
Forestier disease DISH : See Diffuse Ideopathic Skeletal Hyperostosis.
Forestiers disease : See Diffuse Ideopathic Skeletal Hyperostosis.
Forestier’s disease : See Diffuse Ideopathic Skeletal Hyperostosis.
Fragile X syndrome : Fragile X syndrome is categorized as a rare disease. Fragile X...
Fragilitas ossium : See Osteogenesis imperfecta.
Fraser Syndrome : Fraser Syndrome is categorized as a rare disease. Fraser Syndrome...
Fraser-François Ayndrome : See Fraser Syndrome.
Friedreich Ataxia : See Friedreich´s Ataxia.
Friedreich´s Ataxia : Friedreich´s Ataxia is categorized as a rare disease. F...
Friedreichs Ataxia : See Friedreich´s Ataxia.
frontal variant FTD : See Pick´s Disease.
Frontotemporal Dementia : Frontotemporal Dementia is categorized as a rare disease....
Frotteurism : Frotteurism refers to a paraphilic interest in rubbing, usually one´...
Fructose 1 6-bisphosphatase : See Fructose-1 6-Bisphosphatase Deficiency.
Fructose 1-6 Biphosphatase deficiency : See Fructose-1 6-Bisphosphatase Deficiency.
Fructose bisphosphatase deficiency : See Fructose-1 6-Bisphosphatase Deficiency.
Fructose malabsorption : Fructose malabsorption is categorized as a rare disease. F...
Fructose-1 6-Bisphosphatase Deficiency : Fructose-1,6-Bisphosphatase Deficiency is ...
Fröhlich Syndrome : See Prune Belly Syndrome.
FSH : See Facioscapulohumeral Muscular Dystrophy.
FSHD : See Facioscapulohumeral Muscular Dystrophy.
FSHMD : See Facioscapulohumeral Muscular Dystrophy.
FTD : See Frontotemporal Dementia.
Fukuyama Congenital Muscular Dystrophy : Fukuyama Congenital Muscular Dystrophy is ...
Fukuyama muscular dystrophy : See Fukuyama Congenital Muscular Dystrophy.
functional amnesia : See Psychogenic amnesia.
fundus flavimaculatus : See Stargardt disease.



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