Disease Name Symbol Acronym
Fabry Disease FBR012 FD
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 OBLFC1
Facial Dermatosis FCL001
Facial Dermoid Cyst FCL034
Facial Diplegia with Paresthesias FCL071
Facial Dysmorphism with Multiple Malformations FCL064
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly FCL079
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature FCL084 FILS
Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs FCL078 FDLAB
Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification FCL080
Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome FCL068
Facial Hemiatrophy FCL003
Facial Hypertrichosis FCL073
Facial Infiltrating Lipomatosis FCL087
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 FPVEPD
Facial Palsy, Familial Recurrent Peripheral FCL065
Facial Paralysis FCL012
Facial Paresis, Hereditary Congenital, 1 FCL030 HCFP1
Facial Paresis, Hereditary Congenital, 2 FCL050 HCFP2
Facial Paresis, Hereditary Congenital, 3 FCL056 HCFP3
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 FSHD1
Facioscapulohumeral Muscular Dystrophy 2 FCS011 FSHD2
Faciothoracogenital Syndrome FCT031
Factitious Disorder FCT008
Factor Ix and Factor Xi, Combined Deficiency of FCT028 MCFD6
Factor V and Factor Viii, Combined Deficiency of, 1 FCT029 F5F8D1
Factor V and Factor Viii, Combined Deficiency of, 2 FCT034 F5F8D2
Factor V and Factor Viii, Combined Deficiency of, with Normal Protein C and Protein C Inhibitor FCT030
Factor V Deficiency FCT006 FA5D
Factor V Excess with Spontaneous Thrombosis FCT024
Factor V Leiden Thrombophilia FCT013
Factor Vii and Factor Viii, Combined Deficiency of FCT025 MCFD4
Factor Vii Deficiency FCT007 FA7D
Factor Viii and Factor Ix, Combined Deficiency of FCT026
Factor Viii Deficiency FCT001
Factor X Deficiency FCT003 FA10D
Factor Xi Deficiency FCT002 FA11D
Factor Xii Deficiency FCT004 FA12D
Factor Xiii Deficiency FCT005
Factor Xiii, a Subunit, Deficiency of FCT032 FA13AD
Factor Xiii, B Subunit, Deficiency of FCT033 FA13BD
Factors Viii, Ix and Xi, Combined Deficiency of FCT027 MCFD5
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 ADANE
Familial Adenomatous Polyposis FML011 FAP
Familial Adenomatous Polyposis 1 FML346 FAP
Familial Adenomatous Polyposis 2 FML347 FAP2
Familial Adenomatous Polyposis 3 FML299 FAP3
Familial Adenomatous Polyposis 4 FML339 FAP4
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 ATFB
Familial Avascular Necrosis of the Femoral Head FML048
Familial Band Heterotopia FML049
Familial Bilateral Striatal Necrosis FML050 FBSN
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 FCU
Familial Cold Autoinflammatory Syndrome 1 FML116 FCAS1
Familial Cold Autoinflammatory Syndrome 2 FML117 FCAS2
Familial Cold Autoinflammatory Syndrome 3 FML253 FCAS3
Familial Cold Autoinflammatory Syndrome 4 FML270 FCAS4
Familial Colorectal Cancer FML053
Familial Colorectal Cancer Type X FML311 FCCTX
Familial Deafness FML056
Familial Drusen FML292 DHRD
Familial Dupuytren Contracture FML226
Familial Episodic Pain Syndrome FML340 FEPS
Familial Expansile Osteolysis FML345 FEO
Familial Gastric Type 1 Neuroendocrine Tumor FML335
Familial Glomangioma FML025
Familial Glucocorticoid Deficiency FML063
Familial Hemangioma FML158
Familial Hemiplegic Migraine FML023 FHM
Familial Hyperaldosteronism FML156 FH
Familial Hyperlipidemia FML035
Familial Hypertension FML187
Familial Hyperthyroidism Due to Mutations in Tsh Receptor FML067
Familial Hypoaldosteronism FML275
Familial Hypocalciuric Hypercalcemia FML068 FBH
Familial Hypopituitarism FML072
Familial Idiopathic Basal Ganglia Calcification FML043 FIBGC
Familial Idiopathic Dilatation of the Right Atrium FML224
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis FML269
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 Hyperparathyroidism FML075 FIHP
Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland FML196
Familial Isolated Pituitary Adenoma FML168 FIPA
Familial Isolated Restrictive Cardiomyopathy FML293
Familial Keratoacanthoma FML223
Familial Lcat Deficiency FML330 FLD
Familial Lipoprotein Lipase Deficiency FML026
Familial Male-Limited Precocious Puberty FML157 GIPP
Familial Mediterranean Fever FML018 ARFMF
Familial Mediterranean Fever, Autosomal Dominant FML344 ADFMF
Familial Monosomy 7 Syndrome FML317
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 OD
Familial Papillary or Follicular Thyroid Carcinoma FML211 FNMTC
Familial Paroxysmal Nonkinesigenic Dyskinesia FML186 PDC
Familial Partial Lipodystrophy FML012 FPL
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 F-PCT
Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis FML327 FHHNC
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 SQTS
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 FAA
Familial Thyroid Dyshormonogenesis FML297
Familial Tumoral Calcinosis FML091
Familial Vesicoureteral Reflux FML284
Familial Wilms Tumor 2 FML094 FWT2
Familiar Fallopian Tube Carcinoma FML007
Familiar Ovarian Carcinoma FML019
Fanconi Anemia, Complementation Group a FNC027 FANCA
Fanconi Anemia, Complementation Group B FNC032 FANCB
Fanconi Anemia, Complementation Group C FNC044 FANCC
Fanconi Anemia, Complementation Group D1 FNC024 FANCD1
Fanconi Anemia, Complementation Group D2 FNC042 FANCD2
Fanconi Anemia, Complementation Group E FNC043 FANCE
Fanconi Anemia, Complementation Group F FNC045 FANCF
Fanconi Anemia, Complementation Group G FNC030 FANCG
Fanconi Anemia, Complementation Group I FNC029 FANCI
Fanconi Anemia, Complementation Group J FNC025 FANCJ
Fanconi Anemia, Complementation Group L FNC028 FANCL
Fanconi Anemia, Complementation Group N FNC023 FANCN
Fanconi Anemia, Complementation Group O FNC048 FANCO
Fanconi Anemia, Complementation Group P FNC046 FANCP
Fanconi Anemia, Complementation Group Q FNC047 FANCQ
Fanconi Anemia, Complementation Group R FNC058 FANCR
Fanconi Anemia, Complementation Group S FNC062 FANCS
Fanconi Anemia, Complementation Group T FNC052 FANCT
Fanconi Anemia, Complementation Group U FNC057 FANCU
Fanconi Anemia, Complementation Group V FNC056 FANCV
Fanconi Anemia, Complementation Group W FNC061 FANCW
Fanconi Renotubular Syndrome 1 FNC026 RFS
Fanconi Renotubular Syndrome 2 FNC034 FRTS2
Fanconi Renotubular Syndrome 3 FNC049 FRTS3
Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young FNC060 FRTS4
Fanconi Syndrome FNC004
Fanconi-Bickel Syndrome FNC009 FBS
Fanconi-Like Syndrome FNC059
Far Eastern Spotted Fever FRS001
Fara Chlupackova Syndrome FRC004
Farber Lipogranulomatosis FRB001 FRBRL
Farmer's Lung FRM003
Farsightedness FRS019
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 FFI
Fatal Infantile Cytochrome C Oxidase Deficiency FTL054
Fatal Infantile Encephalocardiomyopathy FTL003
Fatal Infantile Encephalomyopathy FTL008
Fatal Infantile Hypertonic Myofibrillar Myopathy FTL045
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 NAFLD1
Fatty Liver Disease, Nonalcoholic 2 FTT007
Faulk Epstein Jones Syndrome FLK001
Faye-Petersen-Ward-Carey Syndrome FYP001
Fazio-Londe Disease FZL002 FALOND
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 FIRES
Febrile Seizures FBR031
Febrile Seizures, Familial, 1 FBR073 FEB1
Febrile Seizures, Familial, 10 FBR068 FEB10
Febrile Seizures, Familial, 11 FBR072 FEB11
Febrile Seizures, Familial, 2 FBR075 FEB2
Febrile Seizures, Familial, 4 FBR069 FEB4
Febrile Seizures, Familial, 5 FBR071 FEB5
Febrile Seizures, Familial, 6 FBR074 FEB6
Febrile Seizures, Familial, 7 FBR076 FEB7
Febrile Seizures, Familial, 9 FBR067 FEB9
Febrile Ulceronecrotic Mucha-Habermann Disease FBR022 FUMHD
Fecal Incontinence FCL044
Feigenbaum Bergeron Richardson Syndrome FGN001
Feigenbaum Bergeron Syndrome FGN002
Feingold Syndrome 1 FNG006 FGLDS1
Feingold Syndrome 2 FNG009 FGLDS2
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 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 FFS
Femur Bifid with Monodactylous Ectrodactyly FMR007 GWC
Femur, Unilateral Bifid, with Monodactylous Ectrodactyly FMR017 GWC
Femur-Fibula-Ulna Syndrome FMR016 PFFD
Fenton Wilkinson Toselano Syndrome FNT001
Ferguson-Smith Tumor FRG002
Ferro-Cerebro-Cutaneous Syndrome FRR002
Fetal Adenoma FTL005
Fetal Akinesia Deformation Sequence FTL009 FADS
Fetal Akinesia Syndrome, X-Linked FTL066
Fetal Alcohol Spectrum Disorder FTL006 FASD
Fetal Alcohol Syndrome FTL001 FAS
Fetal Aminopterin Syndrome FTL011
Fetal and Neonatal Alloimmune Thrombocytopenia FTL012 NAIT
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 HPFH
Fetal Hemoglobin Quantitative Trait Locus 2 FTL036
Fetal Hemoglobin Quantitative Trait Locus 3 FTL035 FCPX
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 FIDD
Fetal Left Ventricular Aneurysm FTL020
Fetal Lung Interstitial Tumor FTL048 FLIT
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 FGS2
Fg Syndrome 3 FGS003 FGS3
Fg Syndrome 4 FGS004 FGS4
Fg Syndrome 5 FGS006 FGS5
Fgfr-Related Craniosynostosis Syndromes FGF001
Fibrillary Astrocytoma FBR008
Fibrillary Glomerulonephritis FBR085
Fibrinogen Deficiency, Congenital FBR023
Fibrinolytic Defect FBR052
Fibro-Adipose Vascular Anomaly FBR090 FAVA
Fibroblastic Liposarcoma FBR004
Fibroblastic Rheumatism FBR091
Fibrocalculous Pancreatopathy FBR065 FCPD
Fibrocartilaginous Embolism FBR024
Fibrochondrogenesis FBR025 FBCG1
Fibrochondrogenesis 1 FBR029 FBCG1
Fibrochondrogenesis 2 FBR030 FBCG2
Fibrodysplasia Ossificans Progressiva FBR011 FOP
Fibroepithelial Basal Cell Carcinoma FBR015
Fibroepithelial Polyp of the Anus FBR006
Fibroepithelial Polyp of Urethra FBR005
Fibrogenesis Imperfecta Ossium FBR010
Fibrolamellar Carcinoma FBR086 FHCC
Fibromatosis FBR019
Fibromatosis Multiple Non Ossifying FBR026
Fibromatosis, Gingival, 1 FBR084 GINGF1
Fibromatosis, Gingival, 2 FBR079 GGF2
Fibromatosis, Gingival, 3 FBR077 GGF3
Fibromatosis, Gingival, 4 FBR080 GGF4
Fibromatosis, Gingival, 5 FBR092 GINGF5
Fibromatosis, Gingival, with Distinctive Facies FBR087
Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation FBR095
Fibromatosis, Gingival, with Progressive Deafness FBR088 GFD
Fibromuscular Dysplasia FBR032 FMD
Fibromyalgia FBR047 FMS
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 CFEOM1
Fibrosis of Extraocular Muscles, Congenital, 2 FBR050 CFEOM2
Fibrosis of Extraocular Muscles, Congenital, 3a, with or Without Extraocular Involvement FBR094 CFEOM3A
Fibrosis of Extraocular Muscles, Congenital, 3c FBR081
Fibrosis of Extraocular Muscles, Congenital, 5 FBR078 CFEOM5
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 FUHRS
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 DPS
Fibular Hypoplasia Scapulo Pelvic Dysplasia Absent FBL007
Fibuloulnar Aplasia or Hypoplasia with Renal Abnormalities FBL018
Ficolin 3 Deficiency FCL083 FCN3D
Fiedler's Myocarditis FDL001
Filamentary Keratitis FLM001
Filarial Elephantiasis FLR001
Filariasis FLR002
Filippi Syndrome FLP001 FLPIS
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 FED
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 FRFB
Flinders Island Spotted Fever FLN001 FISF
Flna-Related Periventricular Nodular Heterotopia FLN007 BPNH
Flnb-Related Disorders FLN002
Floating-Harbor Syndrome FLT006 FLHS
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 FXPOI
Focal Acral Hyperkeratosis FCL040
Focal Alopecia Congenital Megalencephaly FCL020
Focal Chorioretinitis FCL013
Focal Cortical Dysplasia, Type Ii FCL081 FCORD2
Focal Dermal Hypoplasia FCL009 FODH
Focal Dystonia FCL022 FTSD
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 FFDD
Focal Facial Dermal Dysplasia 1, Brauer Type FCL067 FFDD1
Focal Facial Dermal Dysplasia 2, Brauer-Setleis Type FCL066 FFDD2
Focal Facial Dermal Dysplasia 3, Setleis Type FCL045 FFDD3
Focal Facial Dermal Dysplasia 4 FCL046 FFDD4
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 FGS
Focal Segmental Glomerulosclerosis 1 FCL025 FSGS1
Focal Segmental Glomerulosclerosis 2 FCL026 FSGS2
Focal Segmental Glomerulosclerosis 3 FCL027 FSGS3
Focal Segmental Glomerulosclerosis 4 FCL082 FSGS4
Focal Segmental Glomerulosclerosis 5 FCL028 FSGS5
Focal Segmental Glomerulosclerosis 6 FCL043 FSGS6
Focal Segmental Glomerulosclerosis 7 FCL085 FSGS7
Focal Segmental Glomerulosclerosis 8 FCL053 FSGS8
Focal Segmental Glomerulosclerosis 9 FCL055 FSGS9
Foix Chavany Marie Syndrome FXC001
Foix-Alajouanine Syndrome FXL001
Folate Level in Erythrocytes FLT012
Folate Malabsorption, Hereditary FLT009 HFM
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 FL1
Follicular Lymphoreticuloma FLL038
Follicular Mucinosis FLL019
Folliculitis FLL008
Folliculotropic Mycosis Fungoides FLL042
Fontaine Farriaux Blanckaert Syndrome FNT002
Fontaine Progeroid Syndrome FNT005 FPS
Food Allergy FDL002
Foodborne Botulism FDB001
Foot Drop FTD001
Foramen Magnum Meningioma FRM004
Form Agnosia FRM002
Formaldehyde Allergic Contact Dermatitis FRM010
Formaldehyde Poisoning FRM006
Forsythe-Wakeling Syndrome FRS010 FWS
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 FVH1
Foveal Hypoplasia 2 FVL008 FVH2
Fox-Fordyce Disease FXF002
Foxg1 Syndrome FXG001
Foxp2-Related Speech and Language Disorders FXP001 CAS
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 FXS
Fragile X Syndrome Type 1 FRG004
Fragile X Syndrome Type 2 FRG005
Fragile X Syndrome Type 3 FRG006
Fragile X Tremor/ataxia Syndrome FRG010 FXTAS
Fragile X-Associated Tremor/ataxia Syndrome FRG008 FXTAS
Franceschini Vardeu Guala Syndrome FRN015
Frank-Ter Haar Syndrome FRN039 FTHS
Fraser Jequier Chen Syndrome FRS005
Fraser Syndrome 1 FRS014 FRASRS1
Fraser Syndrome 2 FRS016 FRASRS2
Fraser Syndrome 3 FRS015 FRASRS3
Fraser-Like Syndrome FRS017
Frasier Syndrome FRS002 FS
Fraxd FRX001 FRAXD
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 FRDA
Friedreich Ataxia 2 FRD006 FRDA2
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 NYS1
Froelich Syndrome FRL002
Frontal Convexity Meningioma FRN003
Frontal Encephalocele FRN037
Frontal Fibrosing Alopecia FRN020 FFA
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 FFND
Frontometaphyseal Dysplasia FRN012 FMD
Frontometaphyseal Dysplasia 1 FRN049 FMD1
Frontometaphyseal Dysplasia 2 FRN048 FMD2
Frontonasal Arteriovenous Malformation FRN038
Frontonasal Dysplasia 1 FRN036 FND1
Frontonasal Dysplasia 2 FRN033 FND2
Frontonasal Dysplasia 3 FRN032 FND3
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-Bifid Nose-Upper Limb Anomalies Syndrome FRN052
Frontonasal Dysplasia-Severe Microphthalmia-Severe Facial Clefting Syndrome FRN042 FND3
Frontoocular Syndrome FRN050
Frontotemporal Dementia FRN006 FTD
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 FRN044 FTDALS1
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 FRN040 FTDALS2
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 FRN043 FTDALS3
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 FRN045 FTDALS4
Frontotemporal Dementia with Parkinsonism-17 FRN030 DDPAC
Frontotemporal Dementia, Chromosome 3-Linked FRN013 FTD3
Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related FRN051 UP-FTD
Froster-Huch Syndrome FRS008
Frozen Shoulder FRZ001
Fructose and Galactose Intolerance FRC012
Fructose Intolerance, Hereditary FRC011 HFI
Fructose Utilization FRC013
Fructose-1,6-Bisphosphatase Deficiency FRC001 FBP1D
Fructosuria, Essential FRC005 FRUCT
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 FRNS
Fuchs' Endothelial Dystrophy FCH001 FCED
Fuchs' Heterochromic Uveitis FCH002 FHI
Fucosidase Regulator FCS014 FUCT
Fucosidosis FCS002 FUCA1D
Fucosidosis Type 1 FCS008
Fucosyltransferase 6 Deficiency FCS013
Fukuda Miyanomae Nakata Syndrome FKD001
Fukuyama Type Muscular Dystrophy FKY002 FCMD
Fulminant Viral Hepatitis FLM003
Fumarase Deficiency FMR004 FMRD
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 FALBI
Fundus Dystrophy FND002
Fundus Dystrophy, Pseudoinflammatory, Recessive Form FND006
Fundus Pulverulentus FND005
Fungal Esophagitis FNG003
Fungal Gastritis FNG002
Fungal Keratitis FNG016
Fungal Meningitis FNG004
Fungal Myositis FNG013
Funisitis FNS001
Fuqua Berkovitz Syndrome FQB001
Furunculous Myiasis FRN028
Fusariosis FSR001
Futcher Line FTC001
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