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 |
|