| Disease Name |
Symbol |
Acronym |
| Fabry Disease |
FBR012 |
FD |
| Facial Abnormalities, Kyphoscoliosis, and Mental Retardation |
FCL076 |
|
| Facial Arteriovenous Malformation |
FCL058 |
|
| Facial Cleft |
FCL090 |
|
| 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, Hypertrichosis, Epilepsy, Intellectual/developmental Delay, and Gingival Overgrowth Syndrome |
FCL088 |
FHEIG |
| 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 |
CIL-F |
| 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 |
F8F9D |
| 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 |
FAP1 |
| 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 Adult Myoclonic Epilepsy |
FML363 |
FAM |
| Familial Alzheimer-Like Prion Disease |
FML202 |
|
| Familial Amyloidosis, Finnish Type |
FML249 |
|
| Familial Anetoderma |
FML205 |
|
| Familial Apolipoprotein A5 Deficiency |
FML360 |
|
| Familial Apolipoprotein C-Ii Deficiency |
FML285 |
|
| 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 Capillaro-Venous Leptomeningeal Angiomatosis |
FML051 |
|
| Familial Caudal Dysgenesis |
FML329 |
|
| Familial Cerebral Saccular Aneurysm |
FML206 |
|
| Familial Cervical Artery Dissection |
FML325 |
|
| Familial Chilblain Lupus |
FML337 |
|
| Familial Chylomicronemia Due to Inhibition of Lipoprotein Lipase Activity |
FML359 |
|
| 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 Creutzfeld-Jakob Disease |
FML349 |
|
| Familial Cystic Renal Disease |
FML358 |
|
| Familial Deafness |
FML056 |
|
| Familial Drusen |
FML292 |
DHRD |
| Familial Dupuytren Contracture |
FML226 |
|
| Familial Episodic Pain Syndrome |
FML340 |
FEPS |
| Familial Expansile Osteolysis |
FML345 |
FEO |
| Familial Febrile Seizures |
FML350 |
FEB |
| 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 Hypercholesterolemia |
FML021 |
FH |
| Familial Hyperlipidemia |
FML035 |
|
| Familial Hypertension |
FML187 |
|
| Familial Hypoaldosteronism |
FML275 |
|
| Familial Hypocalciuric Hypercalcemia |
FML068 |
FBH |
| Familial Idiopathic Dilatation of the Right Atrium |
FML224 |
|
| Familial Infantile Bilateral Striatal Necrosis |
FML309 |
|
| Familial Intrahepatic Cholestasis |
FML355 |
|
| 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 |
FML362 |
FIH |
| Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland |
FML196 |
|
| Familial Isolated Pituitary Adenoma |
FML168 |
FIPA |
| Familial Isolated Restrictive Cardiomyopathy |
FML293 |
|
| Familial Isolated Trichomegaly |
FML286 |
|
| Familial Keratoacanthoma |
FML223 |
|
| Familial Lcat Deficiency |
FML330 |
FLD |
| Familial Lipoprotein Lipase Deficiency |
FML026 |
|
| Familial Long Qt Syndrome |
FML191 |
|
| Familial Mediterranean Fever |
FML018 |
FMF |
| Familial Mediterranean Fever, Autosomal Dominant |
FML344 |
ADFMF |
| Familial Monosomy 7 Syndrome |
FML317 |
|
| Familial Nasal Acilia |
FML079 |
|
| Familial Nephrotic Syndrome |
FML015 |
|
| Familial Nonmedullary Thyroid Carcinoma |
FML354 |
|
| Familial Omphalocele Syndrome with Facial Dysmorphism |
FML200 |
|
| Familial or Sporadic Hemiplegic Migraine |
FML306 |
|
| Familial Osteochondritis Dissecans |
FML169 |
OD |
| Familial Ovarian Cancer |
FML353 |
|
| 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 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 Scaphocephaly Syndrome |
FML352 |
|
| Familial Short Qt Syndrome |
FML294 |
SQTS |
| Familial Sick Sinus Syndrome |
FML272 |
|
| Familial Spastic Paralysis |
FML160 |
|
| Familial Streblodactyly |
FML088 |
|
| Familial Syringomyelia |
FML255 |
|
| Familial Thoracic Aortic Aneurysm and Aortic Dissection |
FML364 |
FAA |
| Familial Thyroid Dyshormonogenesis |
FML297 |
|
| Familial Tumoral Calcinosis |
FML091 |
|
| Familial Vesicoureteral Reflux |
FML284 |
|
| Familial Wilms Tumor 2 |
FML094 |
FWT2 |
| Familial Woolly Hair Syndrome |
FML361 |
|
| Familiar Fallopian Tube Carcinoma |
FML007 |
|
| Familiar or Sporadic Hemiplegic Migraine |
FML365 |
|
| 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 |
FRTS1 |
| 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 Renotubular Syndrome 5 |
FNC066 |
FRTS5 |
| 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 |
|
| Fars2 Deficiency |
FRS020 |
|
| 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 |
FIQTL1 |
| Fasting Plasma Glucose Level Quantitative Trait Locus 1 |
FST012 |
FGQTL1 |
| Fasting Plasma Glucose Level Quantitative Trait Locus 2 |
FST013 |
FGQTL2 |
| Fasting Plasma Glucose Level Quantitative Trait Locus 3 |
FST014 |
FGQTL3 |
| Fasting Plasma Glucose Level Quantitative Trait Locus 4 |
FST016 |
FGQTL4 |
| Fasting Plasma Glucose Level Quantitative Trait Locus 5 |
FST017 |
FGQTL5 |
| Fasting Plasma Glucose Level Quantitative Trait Locus 6 |
FST015 |
FGQTL6 |
| Fastkd2-Related Infantile Mitochondrial Encephalomyopathy |
FST011 |
|
| Fat Necrosis of Breast |
FTN001 |
|
| Fatal Familial Insomnia |
FTL002 |
FFI |
| Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency |
FTL068 |
|
| Fatal Infantile Encephalomyopathy |
FTL008 |
|
| Fatal Infantile Hypertonic Myofibrillar Myopathy |
FTL045 |
|
| Fatal Post-Viral Neurodegenerative Disorder |
FTL051 |
|
| Fatty Acid Oxidation and Ketogenesis Disorder with Dilated Cardiomyopathy |
FTT009 |
|
| Fatty Acid Oxidation and Ketogenesis Disorder with Hypertrophic Cardiomyopathy |
FTT010 |
|
| Fatty Liver Disease |
FTT001 |
|
| Fatty Liver Disease, Nonalcoholic 1 |
FTT008 |
NAFLD1 |
| Fatty Liver Disease, Nonalcoholic 2 |
FTT007 |
NAFLD2 |
| 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 |
|
| 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, 8 |
FBR070 |
FEB8 |
| Febrile Seizures, Familial, 9 |
FBR067 |
FEB9 |
| Febrile Ulceronecrotic Mucha-Habermann Disease |
FBR022 |
FUMHD |
| 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 an Implantation Defect of Genetic Origin |
FML357 |
|
| 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 1 |
FTL069 |
FADS1 |
| Fetal Akinesia Deformation Sequence 2 |
FTL070 |
FADS2 |
| Fetal Akinesia Deformation Sequence 3 |
FTL071 |
FADS3 |
| Fetal Akinesia Deformation Sequence 4 |
FTL072 |
FADS4 |
| 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 Anticonvulsant Syndrome |
FTL073 |
FACS |
| Fetal Brain Disruption Sequence |
FTL014 |
|
| Fetal Carbamazepine Syndrome |
FTL049 |
|
| Fetal Encasement Syndrome |
FTL075 |
COCOS |
| Fetal Enterovirus Syndrome |
FTL017 |
|
| Fetal Erythroblastosis |
FTL004 |
|
| Fetal Hemoglobin Quantitative Trait Locus 1 |
FTL033 |
HBFQTL1 |
| Fetal Hemoglobin Quantitative Trait Locus 2 |
FTL036 |
HBFQTL2 |
| Fetal Hemoglobin Quantitative Trait Locus 3 |
FTL035 |
HBFQTL3 |
| Fetal Hemoglobin Quantitative Trait Locus 4 |
FTL034 |
HBFQTL4 |
| Fetal Hemoglobin Quantitative Trait Locus 5 |
FTL065 |
HBFQTL5 |
| Fetal Hemoglobin Quantitative Trait Locus 6 |
FTL067 |
HBFQTL6 |
| Fetal Hydantoin Syndrome |
FTL007 |
|
| Fetal Indomethacin Syndrome |
FTL018 |
|
| Fetal Iodine Deficiency Disorder |
FTL062 |
FIDD |
| Fetal Left Ventricular Aneurysm |
FTL020 |
|
| Fetal Lower Urinary Tract Obstruction |
FTL074 |
LUTO |
| 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 |
|
| Fever-Associated Acute Infantile Liver Failure Syndrome |
FVR002 |
|
| Fg Syndrome 2 |
FGS002 |
FGS2 |
| Fg Syndrome 3 |
FGS003 |
FGS3 |
| Fg Syndrome 4 |
FGS004 |
FGS4 |
| Fg Syndrome 5 |
FGS006 |
FGS5 |
| Fgfr Craniosynostosis Syndromes |
FGF014 |
|
| Fgfr3-Related Chondrodysplasia |
FGF013 |
|
| Fh Tumor Predisposition Syndrome |
FHT001 |
HLRCC |
| 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 |
|
| 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 |
|
| Fibrohistiocytic Inflammatory Pseudotumor of the Liver |
FBR098 |
|
| Fibrolamellar Carcinoma |
FBR086 |
FHCC |
| Fibroma |
FBR054 |
|
| Fibromatosis |
FBR019 |
|
| Fibromatosis Multiple Non Ossifying |
FBR026 |
|
| Fibromatosis, Gingival, 1 |
FBR084 |
GINGF1 |
| Fibromatosis, Gingival, 2 |
FBR079 |
GINGF2 |
| Fibromatosis, Gingival, 3 |
FBR077 |
GINGF3 |
| Fibromatosis, Gingival, 4 |
FBR080 |
GINGF4 |
| 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 |
FMDA |
| 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 |
CFEOM3C |
| Fibrosis of Extraocular Muscles, Congenital, 5 |
FBR078 |
CFEOM5 |
| Fibrosis of Extraocular Muscles, Congenital, with Synergistic Divergence |
FBR096 |
|
| Fibrosis, Neurodegeneration, and Cerebral Angiomatosis |
FBR097 |
FINCA |
| 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 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 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 |
|
| Filamin-Related Bone Disorder |
FLM004 |
|
| 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 Walson Mellor Syndrome |
FTZ004 |
|
| Fitzsimmons-Guilbert Syndrome |
FTZ005 |
|
| Fixed Drug Eruption |
FXD003 |
|
| Fkbp14 Kyphoscoliotic Ehlers-Danlos Syndrome |
FKB002 |
|
| 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 Disorders |
FLN009 |
|
| 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 |
|
| Flushing of Ears and Somnolence |
FLS002 |
|
| Flying Phobia |
FLY001 |
|
| Flynn-Aird Syndrome |
FLY003 |
|
| Fmr1 Disorders |
FMR019 |
|
| Focal Acral Hyperkeratosis |
FCL040 |
|
| Focal Alopecia Congenital Megalencephaly |
FCL020 |
|
| Focal Chorioretinitis |
FCL013 |
|
| Focal Cortical Dysplasia, Type Ii |
FCL081 |
FCORD2 |
| Focal Dermal Hypoplasia |
FCL009 |
FDH |
| 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 |
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 Keratoderma |
FCL029 |
|
| 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 |
| Fowler Urethral Sphincter Dysfunction Syndrome |
FWL003 |
|
| Fox-Fordyce Disease |
FXF002 |
|
| Foxg1 Syndrome |
FXG001 |
|
| Foxp2-Related Speech and Language Disorders |
FXP001 |
|
| Fragile Site 10q23 |
FRG012 |
|
| Fragile Site 10q25 |
FRG015 |
FRA10B |
| Fragile Site 11b |
FRG018 |
FRA11B |
| Fragile Site 17p12 |
FRG017 |
|
| Fragile Site 20p11 |
FRG014 |
|
| Fragile Site 9q32 |
FRG016 |
|
| Fragile Site, Distamycin a Type, Rare, Fra(16)(q22.1) |
FRG013 |
FRA16B |
| 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 |
|
| Frem1 Autosomal Recessive Disorders |
FRM011 |
|
| Frenkel Russe Syndrome |
FRN018 |
|
| Frias Syndrome |
FRS007 |
|
| Friedreich Ataxia |
FRD001 |
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 Benign Neoplasm |
FRN058 |
|
| 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-Bifid Nose-Upper Limb Anomalies Syndrome |
FRN052 |
|
| Frontoocular Syndrome |
FRN050 |
|
| Frontotemporal Degeneration with Dementia |
FRN054 |
|
| 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 |
| Frontotemporal Neurodegeneration with Movement Disorder |
FRN053 |
|
| 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 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 |
| Fucosyltransferase 6 Deficiency |
FCS013 |
|
| Fukuda Miyanomae Nakata Syndrome |
FKD001 |
|
| Fukuyama Type Muscular Dystrophy |
FKY002 |
FCMD |
| Fumarase Deficiency |
FMR004 |
FMRD |
| Fumarate Hydratase Deficiency |
FMR011 |
|
| Functional Colonic Disease |
FNC005 |
|
| Functional Diarrhea |
FNC002 |
|
| Functional Gastric Disease |
FNC006 |
|
| Functional Neutrophil Defect |
FNC063 |
|
| Functional Variant of Guillain-Barre Syndrome |
FNC064 |
|
| Functioning Gonadotropic Adenoma |
FNC050 |
|
| Functioning Neuroendocrine Tumor of Pancreas |
FNC065 |
|
| 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 Infectious Disease |
FNG017 |
|
| Fungal Keratitis |
FNG016 |
|
| Fungal Meningitis |
FNG004 |
|
| Fungal Myositis |
FNG013 |
|
| Funisitis |
FNS001 |
|
| Fuqua Berkovitz Syndrome |
FQB001 |
|
| Furuncular Myiasis Due to Cordylobia Anthropophaga |
FRN057 |
|
| Furuncular Myiasis Due to Cordylobia Rodhaini |
FRN055 |
|
| Furuncular Myiasis Due to Dermatobia Hominis |
FRN056 |
|
| Furunculous Myiasis |
FRN028 |
|
| Fusariosis |
FSR001 |
|
| Futcher Line |
FTC001 |
|
