Disease Name Symbol Acronym
Fabry Disease FBR012
Facial Abnormalities, Kyphoscoliosis, and Mental Retardation FCL076
Facial Arteriovenous Malformation FCL058
Facial Asymmetry Temporal Seizures FCL060
Facial Clefting Corpus Callosum Agenesis FCL018
Facial Clefting, Oblique, 1 FCL047
Facial Dermatosis FCL001
Facial Dermoid Cyst FCL034
Facial Diplegia with Paresthesias FCL071
Facial Dysmorphism with Multiple Malformations FCL064
Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome FCL068
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly FCL079
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature FCL084
Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs FCL078
Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification FCL080
Facial Hemiatrophy FCL003
Facial Hypertrichosis FCL073
Facial Nerve Disease FCL011
Facial Nerve Neoplasm FCL002
Facial Neuralgia FCL007
Facial Onset Sensory and Motor Neuronopathy FCL042
Facial Palsy, Congenital, with Ptosis and Velopharyngeal Dysfunction FCL086
Facial Palsy, Familial Recurrent Peripheral FCL065
Facial Paralysis FCL012
Facial Paresis, Hereditary Congenital, 1 FCL030
Facial Paresis, Hereditary Congenital, 2 FCL050
Facial Paresis, Hereditary Congenital, 3 FCL056
Facial Spasm FCL074
Facio Digito Genital Syndrome Recessive Form FCD001
Facio Skeletal Genital Syndrome Rippberger Type FCS007
Faciocardiomelic Dysplasia, Lethal FCC003
Faciocardiomelic Syndrome FCC004
Faciocardiorenal Syndrome FCC002
Faciodigitogenital Syndrome, Autosomal Recessive FCD002
Facioscapulohumeral Muscular Dystrophy 1 FCS012
Facioscapulohumeral Muscular Dystrophy 2 FCS011
Faciothoracogenital Syndrome FCT031
Factitious Disorder FCT008
Factor Ix and Factor Xi, Combined Deficiency of FCT028
Factor V and Factor Viii, Combined Deficiency of, 1 FCT029
Factor V and Factor Viii, Combined Deficiency of, 2 FCT034
Factor V and Factor Viii, Combined Deficiency of, with Normal Protein C and Protein C Inhibitor FCT030
Factor V Deficiency FCT006
Factor V Excess with Spontaneous Thrombosis FCT024
Factor V Leiden Thrombophilia FCT013
Factor Vii and Factor Viii, Combined Deficiency of FCT025
Factor Vii Deficiency FCT007
Factor Viii and Factor Ix, Combined Deficiency of FCT026
Factor Viii Deficiency FCT001
Factor X Deficiency FCT003
Factor Xi Deficiency FCT002
Factor Xii Deficiency FCT004
Factor Xiii Deficiency FCT005
Factor Xiii, a Subunit, Deficiency of FCT032
Factor Xiii, B Subunit, Deficiency of FCT033
Factors Viii, Ix and Xi, Combined Deficiency of FCT027
Failure of Tooth Eruption, Primary FLR007 PFE
Fainting FNT004
Fallopian Tube Adenocarcinoma FLL023
Fallopian Tube Adenofibroma FLL024
Fallopian Tube Adenomatoid Tumor FLL009
Fallopian Tube Adenosarcoma FLL005
Fallopian Tube Benign Neoplasm FLL025
Fallopian Tube Carcinoma FLL027
Fallopian Tube Carcinosarcoma FLL028
Fallopian Tube Clear Cell Adenocarcinoma FLL022
Fallopian Tube Cystadenofibroma FLL012
Fallopian Tube Disease FLL029
Fallopian Tube Endometrioid Adenocarcinoma FLL003
Fallopian Tube Endometriosis FLL006
Fallopian Tube Germ Cell Cancer FLL030
Fallopian Tube Gestational Choriocarcinoma FLL011
Fallopian Tube Leiomyoma FLL010
Fallopian Tube Leiomyosarcoma FLL007
Fallopian Tube Mucinous Adenocarcinoma FLL001
Fallopian Tube Mucinous Tumor FLL002
Fallopian Tube Papillary Adenocarcinoma FLL016
Fallopian Tube Serous Adenocarcinoma FLL015
Fallopian Tube Serous Papilloma FLL004
Fallopian Tube Squamous Cell Carcinoma FLL017
Fallopian Tube Teratoma FLL018
Fallopian Tube Transitional Cell Carcinoma FLL014
Fallot Complex with Severe Mental and Growth Retardation FLL034
Familial Abdominal Aortic Aneurysm FML305
Familial Acute Myeloid Leukemia with Mutated Cebpa FML155
Familial Acute Necrotizing Encephalopathy FML258
Familial Adenomatous Polyposis FML011
Familial Adenomatous Polyposis 1 FML346
Familial Adenomatous Polyposis 2 FML347
Familial Adenomatous Polyposis 3 FML299
Familial Adenomatous Polyposis 4 FML339
Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion FML254
Familial Alzheimer-Like Prion Disease FML202
Familial Amyloidosis, Finnish Type FML249
Familial Anetoderma FML205
Familial Arteriosclerotic Leukoencephalopathy, Alopecia, Lumbago Without Arterial Hypertension FML047
Familial Atrial Fibrillation FML001
Familial Avascular Necrosis of the Femoral Head FML048
Familial Band Heterotopia FML049
Familial Bicuspid Aortic Valve FML264
Familial Bilateral Striatal Necrosis FML050
Familial Calcium Pyrophosphate Deposition FML307
Familial Candidiasis FML334
Familial Capillaro-Venous Leptomeningeal Angiomatosis FML051
Familial Caudal Dysgenesis FML329
Familial Cerebral Saccular Aneurysm FML206
Familial Cervical Artery Dissection FML325
Familial Chilblain Lupus FML337
Familial Clubfoot with or Without Associated Lower Limb Anomalies FML194
Familial Cold Autoinflammatory Syndrome FML052
Familial Cold Autoinflammatory Syndrome 1 FML116 FCAS1
Familial Cold Autoinflammatory Syndrome 2 FML117
Familial Cold Autoinflammatory Syndrome 3 FML253
Familial Cold Autoinflammatory Syndrome 4 FML270
Familial Colorectal Cancer FML053
Familial Colorectal Cancer Type X FML311
Familial Deafness FML056
Familial Drusen FML292
Familial Dupuytren Contracture FML226
Familial Episodic Pain Syndrome FML340
Familial Expansile Osteolysis FML345
Familial Gastric Type 1 Neuroendocrine Tumor FML335
Familial Glomangioma FML025
Familial Glucocorticoid Deficiency FML063
Familial Hemangioma FML158
Familial Hemiplegic Migraine FML023
Familial Hyperaldosteronism FML156
Familial Hyperlipidemia FML035
Familial Hypertension FML187
Familial Hyperthyroidism Due to Mutations in Tsh Receptor FML067
Familial Hypoaldosteronism FML275
Familial Hypocalciuric Hypercalcemia FML068
Familial Hypopituitarism FML072
Familial Idiopathic Basal Ganglia Calcification FML043
Familial Idiopathic Dilatation of the Right Atrium FML224
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Proliferation FML230
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis FML267
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes FML268
Familial Infantile Bilateral Striatal Necrosis FML309
Familial Interstitial Fibrosis FML074
Familial Isolated Arrhythmogenic Right Ventricular Dysplasia FML279
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form FML214
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form FML215
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form FML213
Familial Isolated Clinodactyly of Fingers FML216
Familial Isolated Dilated Cardiomyopathy FML304
Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland FML196
Familial Isolated Pituitary Adenoma FML168
Familial Isolated Restrictive Cardiomyopathy FML293
Familial Juvenile Hyperuricaemic Nephropathy FML076
Familial Keratoacanthoma FML223
Familial Lcat Deficiency FML330
Familial Lipoprotein Lipase Deficiency FML026
Familial Male-Limited Precocious Puberty FML157
Familial Mediterranean Fever FML018
Familial Mediterranean Fever, Autosomal Dominant FML344
Familial Monosomy 7 Syndrome FML317
Familial Myelofibrosis FML078
Familial Nasal Acilia FML079
Familial Nephrotic Syndrome FML015
Familial Omphalocele Syndrome with Facial Dysmorphism FML200
Familial or Sporadic Hemiplegic Migraine FML306
Familial Osteochondritis Dissecans FML169
Familial Papillary or Follicular Thyroid Carcinoma FML211
Familial Paroxysmal Nonkinesigenic Dyskinesia FML186
Familial Partial Lipodystrophy FML012
Familial Partial Lipodystrophy Due to Akt2 Mutations FML227
Familial Partial Paralysis FML082
Familial Patent Arterial Duct FML336
Familial Periodic Paralyses FML159
Familial Periodic Paralysis FML036
Familial Pityriasis Rubra Pilaris FML348
Familial Porencephaly FML084
Familial Porphyria Cutanea Tarda FML324
Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis FML327
Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia FML315
Familial Progressive Cardiac Conduction Defect FML250
Familial Progressive Hyperpigmentation FML313
Familial Pulmonary Arterial Hypertension Leucopenia and Atrial Septal Defect FML086
Familial Renal Oncocytoma FML028
Familial Renal Papillary Carcinoma FML029
Familial Retinoblastoma FML008
Familial Short Qt Syndrome FML294
Familial Sick Sinus Syndrome FML272
Familial Spastic Paralysis FML160
Familial Stomach Cancer FML321
Familial Streblodactyly FML088
Familial Syringomyelia FML255
Familial Thoracic Aortic Aneurysm and Dissection FML089
Familial Thyroid Dyshormonogenesis FML297
Familial Tumoral Calcinosis FML091
Familial Vesicoureteral Reflux FML284
Familial Wilms Tumor 2 FML094
Familiar Fallopian Tube Carcinoma FML007
Familiar Ovarian Carcinoma FML019
Fanconi Anemia, Complementation Group a FNC027
Fanconi Anemia, Complementation Group B FNC032
Fanconi Anemia, Complementation Group C FNC044
Fanconi Anemia, Complementation Group D1 FNC024
Fanconi Anemia, Complementation Group D2 FNC042
Fanconi Anemia, Complementation Group E FNC043
Fanconi Anemia, Complementation Group F FNC045
Fanconi Anemia, Complementation Group G FNC030
Fanconi Anemia, Complementation Group I FNC029
Fanconi Anemia, Complementation Group J FNC025
Fanconi Anemia, Complementation Group L FNC028
Fanconi Anemia, Complementation Group N FNC023
Fanconi Anemia, Complementation Group O FNC048
Fanconi Anemia, Complementation Group P FNC046
Fanconi Anemia, Complementation Group Q FNC047
Fanconi Anemia, Complementation Group R FNC058
Fanconi Anemia, Complementation Group S FNC062
Fanconi Anemia, Complementation Group T FNC052
Fanconi Anemia, Complementation Group U FNC057
Fanconi Anemia, Complementation Group V FNC056
Fanconi Anemia, Complementation Group W FNC061
Fanconi Renotubular Syndrome 1 FNC026
Fanconi Renotubular Syndrome 2 FNC034
Fanconi Renotubular Syndrome 3 FNC049
Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young FNC060
Fanconi Syndrome FNC004
Fanconi-Bickel Syndrome FNC009
Fanconi-Like Syndrome FNC059
Far Eastern Spotted Fever FRS001
Fara Chlupackova Syndrome FRC004
Farber Lipogranulomatosis FRB001
Farmer's Lung FRM003
Fascial Dystrophy, Congenital FSC007
Fasciitis FSC004
Fascioliasis FSC002
Fascioloidiasis FSC001
Fasciolopsiasis FSC003
Fasting Hypoglycemia FST010
Fasting Insulin Level Quantitative Trait Locus 1 FST003
Fasting Plasma Glucose Level Quantitative Trait Locus 1 FST012
Fasting Plasma Glucose Level Quantitative Trait Locus 2 FST013
Fasting Plasma Glucose Level Quantitative Trait Locus 3 FST014
Fasting Plasma Glucose Level Quantitative Trait Locus 4 FST016
Fasting Plasma Glucose Level Quantitative Trait Locus 5 FST017
Fasting Plasma Glucose Level Quantitative Trait Locus 6 FST015
Fastkd2-Related Infantile Mitochondrial Encephalomyopathy FST011
Fat Necrosis of Breast FTN001
Fatal Familial Insomnia FTL002
Fatal Infantile Cytochrome C Oxidase Deficiency FTL054
Fatal Infantile Encephalocardiomyopathy FTL003
Fatal Infantile Encephalomyopathy FTL008
Fatal Infantile Hypertrophic Cardiomyopathy Due to Mitochondrial Complex I Deficiency FTL050
Fatal Post-Viral Neurodegenerative Disorder FTL051
Fatty Liver Disease FTT001
Fatty Liver Disease, Nonalcoholic 1 FTT008
Fatty Liver Disease, Nonalcoholic 2 FTT007
Faulk Epstein Jones Syndrome FLK001
Faye-Petersen-Ward-Carey Syndrome FYP001
Fazio-Londe Disease FZL002
Fbln1-Related Developmental Delay-Central Nervous System Anomaly-Syndactyly Syndrome FBL015
Fbln5-Related Cutis Laxa FBL003
Fbxl4-Related Encephalomyopathic Mitochondrial Dna Depletion Syndrome FBX003
Febrile Infection-Related Epilepsy Syndrome FBR064
Febrile Seizures FBR031
Febrile Seizures, Familial, 1 FBR073 FEB1
Febrile Seizures, Familial, 10 FBR068
Febrile Seizures, Familial, 11 FBR072
Febrile Seizures, Familial, 2 FBR075
Febrile Seizures, Familial, 4 FBR069
Febrile Seizures, Familial, 5 FBR071
Febrile Seizures, Familial, 6 FBR074
Febrile Seizures, Familial, 7 FBR076
Febrile Seizures, Familial, 9 FBR067
Febrile Ulceronecrotic Mucha-Habermann Disease FBR022
Fecal Incontinence FCL044
Feigenbaum Bergeron Richardson Syndrome FGN001
Feigenbaum Bergeron Syndrome FGN002
Feingold Syndrome 1 FNG006
Feingold Syndrome 2 FNG009
Feingold Trainer Syndrome FNG007
Felty Syndrome FLT011
Female Breast Axillary Tail Cancer FML009
Female Breast Cancer FML037
Female Breast Central Part Cancer FML006
Female Breast Lower-Inner Quadrant Cancer FML013
Female Breast Lower-Outer Quadrant Cancer FML017
Female Breast Nipple and Areola Cancer FML030
Female Breast Upper-Inner Quadrant Cancer FML014
Female Breast Upper-Outer Quadrant Cancer FML033
Female Infertility Due to Oocyte Meiotic Arrest FML343
Female Infertility Due to Zona Pellucida Defect FML266
Female Infertility of Uterine Origin FML002
Female Reproductive Endometrioid Cancer FML005
Female Reproductive Organ Cancer FML038
Female Reproductive System Disease FML039
Female Stress Incontinence FML031
Female Urethral Cancer FML040
Femoral Agenesis/hypoplasia FMR013
Femoral Cancer FMR002
Femoral Neuropathy FMR003
Femoral Vein Thrombophlebitis FMR001
Femoral-Facial Syndrome FMR018
Femur Bifid with Monodactylous Ectrodactyly FMR007
Femur-Fibula-Ulna Syndrome FMR016
Femur, Unilateral Bifid, with Monodactylous Ectrodactyly FMR017
Fenton Wilkinson Toselano Syndrome FNT001
Ferguson-Smith Tumor FRG002
Ferro-Cerebro-Cutaneous Syndrome FRR002
Fetal Adenoma FTL005
Fetal Akinesia Deformation Sequence FTL009
Fetal Akinesia Syndrome, X-Linked FTL066
Fetal Alcohol Spectrum Disorder FTL006
Fetal Alcohol Syndrome FTL001
Fetal Aminopterin Syndrome FTL011
Fetal and Neonatal Alloimmune Thrombocytopenia FTL012
Fetal Brain Disruption Sequence FTL014
Fetal Carbamazepine Syndrome FTL049
Fetal Cytomegalovirus Syndrome FTL044
Fetal Edema FTL016
Fetal Enterovirus Syndrome FTL017
Fetal Erythroblastosis FTL004
Fetal Hemoglobin Quantitative Trait Locus 1 FTL033
Fetal Hemoglobin Quantitative Trait Locus 2 FTL036
Fetal Hemoglobin Quantitative Trait Locus 3 FTL035
Fetal Hemoglobin Quantitative Trait Locus 4 FTL034
Fetal Hemoglobin Quantitative Trait Locus 5 FTL065
Fetal Hemoglobin Quantitative Trait Locus 6 FTL067
Fetal Hydantoin Syndrome FTL007
Fetal Indomethacin Syndrome FTL018
Fetal Iodine Deficiency Disorder FTL062
Fetal Left Ventricular Aneurysm FTL020
Fetal Lung Interstitial Tumor FTL048
Fetal Macrosomia FTL021
Fetal Methylmercury Syndrome FTL064
Fetal Minoxidil Syndrome FTL024
Fetal Nicotine Spectrum Disorder FTL063
Fetal Parainfluenza Virus Type 3 Syndrome FTL025
Fetal Parvovirus Syndrome FTL026
Fetal Phenothiazine Syndrome FTL027
Fetal Retinoid Syndrome FTL028
Fetal Thalidomide Syndrome FTL029
Fetal Trimethadione Syndrome FTL058
Fetishism FTS001
Fever, Familial Lifelong Persistent FVR001
Fg Syndrome 2 FGS002
Fg Syndrome 3 FGS003
Fg Syndrome 4 FGS004
Fg Syndrome 5 FGS006
Fgfr-Related Craniosynostosis Syndromes FGF001
Fibrillary Astrocytoma FBR008
Fibrillary Glomerulonephritis FBR085
Fibrinogen Deficiency, Congenital FBR023
Fibrinolytic Defect FBR052
Fibro-Adipose Vascular Anomaly FBR090
Fibroblastic Liposarcoma FBR004
Fibroblastic Rheumatism FBR091
Fibrocalculous Pancreatopathy FBR065
Fibrocartilaginous Embolism FBR024
Fibrochondrogenesis FBR025
Fibrochondrogenesis 1 FBR029
Fibrochondrogenesis 2 FBR030
Fibrodysplasia Ossificans Progressiva FBR011
Fibroepithelial Basal Cell Carcinoma FBR015
Fibroepithelial Polyp of the Anus FBR006
Fibroepithelial Polyp of Urethra FBR005
Fibrogenesis Imperfecta Ossium FBR010
Fibrolamellar Carcinoma FBR086
Fibromatosis FBR019
Fibromatosis Multiple Non Ossifying FBR026
Fibromatosis, Gingival, 1 FBR084
Fibromatosis, Gingival, 2 FBR079
Fibromatosis, Gingival, 3 FBR077
Fibromatosis, Gingival, 4 FBR080
Fibromatosis, Gingival, 5 FBR092
Fibromatosis, Gingival, with Distinctive Facies FBR087
Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation FBR095
Fibromatosis, Gingival, with Progressive Deafness FBR088
Fibromuscular Dysplasia FBR032
Fibromyalgia FBR047
Fibroosseous Pseudotumor of Digits FBR007
Fibrosarcoma FBR017
Fibrosarcoma of Bone FBR002
Fibrosarcomatous Osteosarcoma FBR013
Fibrosclerosis of Breast FBR016
Fibrosclerosis, Multifocal FBR089
Fibrosing Mediastinitis FBR028
Fibrosis of Extraocular Muscles, Congenital, 1 FBR046
Fibrosis of Extraocular Muscles, Congenital, 2 FBR050
Fibrosis of Extraocular Muscles, Congenital, 3a, with or Without Extraocular Involvement FBR094
Fibrosis of Extraocular Muscles, Congenital, 3c FBR081
Fibrosis of Extraocular Muscles, Congenital, 5 FBR078
Fibrosis of Extraocular Muscles, Congenital, with Synergistic Divergence FBR096
Fibrous Dysplasia FBR009
Fibrous Dysplasia/mccune-Albright Syndrome FBR083
Fibrous Histiocytoma FBR003
Fibrous Meningioma FBR001
Fibrous Synovial Sarcoma FBR014
Fibula Aplasia Complex Brachydactyly FBL004
Fibula, Recurrent Dislocation of Head of FBL019
Fibular Aplasia Ectrodactyly FBL006
Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly FBL008
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome FBL010
Fibular Collateral Ligament Bursitis FBL001
Fibular Dimelia-Diplopodia Syndrome FBL017
Fibular Hemimelia FBL014
Fibular Hypoplasia and Complex Brachydactyly FBL002
Fibular Hypoplasia Scapulo Pelvic Dysplasia Absent FBL007
Fibuloulnar Aplasia or Hypoplasia with Renal Abnormalities FBL018
Ficolin 3 Deficiency FCL083
Fiedler's Myocarditis FDL001
Filamentary Keratitis FLM001
Filarial Elephantiasis FLR001
Filariasis FLR002
Filippi Syndrome FLP001
Finger Agnosia FNG001
Finger Hyperphalangy-Toe Anomalies-Severe Pectus Excavatum Syndrome FNG012
Finger Locking, Recurrent, with Intrauterine Growth Retardation and Proportionate Short Stature FNG014
Fingerprint Body Myopathy FNG010
Fingers, Relative Length of FNG015
First Branchial Cleft Anomaly FRS011
First-Degree Atrioventricular Block FRS012
Fish Allergy FSH003
Fish-Eye Disease FSH001
Fissured Tongue FSS001
Fitz-Hugh-Curtis Syndrome FTZ002
Fitzsimmons Syndrome FTZ003
Fitzsimmons Walson Mellor Syndrome FTZ004
Fitzsimmons-Guilbert Syndrome FTZ005
Fixed Drug Eruption FXD003
Flat Ductal Epithelial Atypia FLT002
Flat Retinoschisis FLT003
Flavimonas Oryzihabitans Infection FLV003
Fleck Retina of Kandori FLC004
Fleck Retina, Familial Benign FLC002
Flinders Island Spotted Fever FLN001
Flna-Related Periventricular Nodular Heterotopia FLN007
Flnb-Related Disorders FLN002
Floating-Harbor Syndrome FLT006
Flood Factor Deficiency FLD005
Floppy Infant Syndrome FLP002
Florid Cemento-Osseous Dysplasia FLR003
Florid Cystic Endosalpingiosis of the Uterus FLR004
Flotch Syndrome FLT007
Flucloxacilline Toxicity FLC003
Flushing of Ears and Somnolence FLS002
Flying Phobia FLY001
Flynn-Aird Syndrome FLY003
Fmr1-Related Disorders FMR005
Fmr1-Related Primary Ovarian Insufficiency FMR009
Focal Acral Hyperkeratosis FCL040
Focal Alopecia Congenital Megalencephaly FCL020
Focal Chorioretinitis FCL013
Focal Cortical Dysplasia, Type Ii FCL081
Focal Dermal Hypoplasia FCL009
Focal Dystonia FCL022
Focal Embolic Glomerulonephritis FCL004
Focal Epilepsy FCL014
Focal Epilepsy-Intellectual Disability-Cerebro-Cerebellar Malformation FCL062
Focal Epithelial Hyperplasia FCL010
Focal Epithelial Hyperplasia of the Oral Mucosa FCL075
Focal Epithelial Hyperplasia, Oral FCL077
Focal Facial Dermal Dysplasia FCL023
Focal Facial Dermal Dysplasia 1, Brauer Type FCL067
Focal Facial Dermal Dysplasia 2, Brauer-Setleis Type FCL066
Focal Facial Dermal Dysplasia 3, Setleis Type FCL045
Focal Facial Dermal Dysplasia 4 FCL046
Focal Hand Dystonia FCL049
Focal Labyrinthitis FCL006
Focal Myositis FCL041
Focal or Multifocal Malformations in Neuronal Migration FCL024
Focal Palmoplantar and Gingival Keratoderma FCL036
Focal Segmental Glomerulosclerosis FCL005
Focal Segmental Glomerulosclerosis 1 FCL025
Focal Segmental Glomerulosclerosis 2 FCL026
Focal Segmental Glomerulosclerosis 3 FCL027
Focal Segmental Glomerulosclerosis 4 FCL082
Focal Segmental Glomerulosclerosis 5 FCL028
Focal Segmental Glomerulosclerosis 6 FCL043
Focal Segmental Glomerulosclerosis 7 FCL085
Focal Segmental Glomerulosclerosis 8 FCL053
Focal Segmental Glomerulosclerosis 9 FCL055
Foix Chavany Marie Syndrome FXC001
Foix-Alajouanine Syndrome FXL001
Folate Level in Erythrocytes FLT012
Folate Malabsorption, Hereditary FLT009
Folic Acid Deficiency Anemia FLC001
Folinic Acid-Responsive Seizures FLN005
Follicular Adenoma FLL031
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts FLL049
Follicular Basal Cell Carcinoma FLL021
Follicular Cholangitis and Pancreatitis FLL045
Follicular Dendritic Cell Sarcoma FLL013
Follicular Infundibulum Tumor FLL020
Follicular Lymphoma FLL037
Follicular Lymphoma 1 FLL041
Follicular Lymphoreticuloma FLL038
Follicular Mucinosis FLL019
Folliculitis FLL008
Folliculotropic Mycosis Fungoides FLL042
Fontaine Farriaux Blanckaert Syndrome FNT002
Fontaine Progeroid Syndrome FNT005
Food Allergy FDL002
Foodborne Botulism FDB001
Foot Drop FTD001
Foramen Magnum Meningioma FRM004
Form Agnosia FRM002
Formaldehyde Poisoning FRM006
Forsythe-Wakeling Syndrome FRS010
Foster-Kennedy Syndrome FST001
Fountain Syndrome FNT003
Fournier Gangrene FRN014
Fourth Branchial Cleft Anomaly FRT004
Fourth Cranial Nerve Palsy FRT001
Fourth Cranial Nerve Palsy, Familial Congenital FRT006
Foveal Hypoplasia 1 FVL006
Foveal Hypoplasia 2 FVL008
Fox-Fordyce Disease FXF002
Foxg1 Syndrome FXG001
Foxp2-Related Speech and Language Disorders FXP001
Fragile Site 10q23 FRG012
Fragile Site 10q25 FRG015
Fragile Site 11b FRG018
Fragile Site 17p12 FRG017
Fragile Site 20p11 FRG014
Fragile Site 9q32 FRG016
Fragile Site, Distamycin a Type, Rare, Fra(16)(q22.1) FRG013
Fragile X Syndrome FRG001
Fragile X Syndrome Type 1 FRG004
Fragile X Syndrome Type 2 FRG005
Fragile X Syndrome Type 3 FRG006
Fragile X Tremor/ataxia Syndrome FRG010
Fragile X-Associated Tremor/ataxia Syndrome FRG008
Franceschini Vardeu Guala Syndrome FRN015
Frank-Ter Haar Syndrome FRN039
Fraser Jequier Chen Syndrome FRS005
Fraser Syndrome 1 FRS014
Fraser Syndrome 2 FRS016
Fraser Syndrome 3 FRS015
Fraser-Like Syndrome FRS017
Frasier Syndrome FRS002
Fraxd FRX001
Fraxf Syndrome FRX003
Free Sialic Acid Storage Disorders FRS004
Freemartinism FRM001
Freesia Flowers, Inability to Smell FRS018
Freiberg's Disease FRB005
Frenkel Russe Syndrome FRN018
Frias Syndrome FRS007
Friedel Heid Grosshans Syndrome FRD003
Friedreich Ataxia 1 FRD012
Friedreich Ataxia 2 FRD006
Friedreich Ataxia and Congenital Glaucoma FRD013
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness FRD011
Frints De Smet Fabry Fryns Syndrome FRN019
Frmd7-Related Infantile Nystagmus FRM005
Froelich Syndrome FRL002
Frontal Convexity Meningioma FRN003
Frontal Encephalocele FRN037
Frontal Fibrosing Alopecia FRN020
Frontal Lobe Neoplasm FRN007
Frontal Sinus Cancer FRN009
Frontal Sinus Inverted Papilloma FRN004
Frontal Sinus Schneiderian Papilloma FRN001
Frontal Sinus Squamous Cell Carcinoma FRN005
Frontal Sinusitis FRN011
Fronto Nasal Malformation Cloacal Exstrophy FRN021
Frontofacionasal Dysplasia FRN022
Frontometaphyseal Dysplasia FRN012
Frontometaphyseal Dysplasia 1 FRN049
Frontometaphyseal Dysplasia 2 FRN048
Frontonasal Arteriovenous Malformation FRN038
Frontonasal Dysplasia 1 FRN036
Frontonasal Dysplasia 2 FRN033
Frontonasal Dysplasia 3 FRN032
Frontonasal Dysplasia Acromelic FRN024
Frontonasal Dysplasia Klippel Feil Syndrome FRN025
Frontonasal Dysplasia Phocomelic Upper Limbs FRN026
Frontonasal Dysplasia with Alar Clefts FRN047
Frontonasal Dysplasia with Alopecia and Genital Anomaly FRN041
Frontonasal Dysplasia-Severe Microphthalmia-Severe Facial Clefting Syndrome FRN042
Frontoocular Syndrome FRN050
Frontotemporal Dementia FRN006
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 FRN044 FTDALS1
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 FRN040
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 FRN043
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 FRN045
Frontotemporal Dementia with Parkinsonism-17 FRN030
Frontotemporal Dementia, Chromosome 3-Linked FRN013
Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related FRN051
Froster-Huch Syndrome FRS008
Frozen Shoulder FRZ001
Fructose and Galactose Intolerance FRC012
Fructose Intolerance, Hereditary FRC011
Fructose Utilization FRC013
Fructose-1,6-Bisphosphatase Deficiency FRC001
Fructosuria, Essential FRC005
Fruit Allergy FRT005
Fryns Fabry Remans Syndrome FRY003
Fryns Hofkens Fabry Syndrome FRY004
Fryns Macrocephaly FRY007
Fryns Microphthalmia Syndrome FRY006
Fryns Smeets Thiry Syndrome FRY005
Fryns Syndrome FRY002
Fuchs' Endothelial Dystrophy FCH001
Fuchs' Heterochromic Uveitis FCH002
Fucosidase Regulator FCS014
Fucosidosis FCS002
Fucosidosis Type 1 FCS008
Fucosyltransferase 6 Deficiency FCS013
Fukuda Miyanomae Nakata Syndrome FKD001
Fukuyama Type Muscular Dystrophy FKY002
Fulminant Viral Hepatitis FLM003
Fumarase Deficiency FMR004
Fumarate Hydratase Deficiency FMR011
Functional Colonic Disease FNC005
Functional Diarrhea FNC002
Functional Gastric Disease FNC006
Functioning Gonadotropic Adenoma FNC050
Functioning Pancreatic Endocrine Tumor FNC012
Functioning Pituitary Adenoma FNC007
Functionless Pituitary Adenoma FNC003
Fundus Albipunctatus FND001
Fundus Dystrophy FND002
Fundus Dystrophy, Pseudoinflammatory, Recessive Form FND006
Fundus Pulverulentus FND005
Fungal Esophagitis FNG003
Fungal Gastritis FNG002
Fungal Meningitis FNG004
Fungal Myositis FNG013
Funisitis FNS001
Fuqua Berkovitz Syndrome FQB001
Furunculous Myiasis FRN028
Fusariosis FSR001
Futcher Line FTC001
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