Disease Name Symbol Acronym
G6pc3 Deficiency G6P001
Gaba Aminotransferase Deficiency GBM001
Gaba-Transaminase Deficiency GBT001
Gabriele-De Vries Syndrome GBR007
Gait Apraxia GTP001
Gait Ataxia with Late Onset Polyneuropathy Syndrome GTT003
Galactokinase Deficiency GLC004
Galactorrhea GLC096
Galactorrhoea-Hyperprolactinaemia GLC025
Galactose Epimerase Deficiency GLC011
Galactosemia GLC006
Galactosialidosis GLC012
Gall Bladder Carcinoma in Situ GLL001
Gallbladder Adenocarcinoma GLL017
Gallbladder Adenoma GLL029
Gallbladder Angiosarcoma GLL002
Gallbladder Cancer GLL018
Gallbladder Disease GLL020
Gallbladder Disease 1 GLL024
Gallbladder Disease 2 GLL025
Gallbladder Disease 3 GLL026
Gallbladder Disease 4 GLL027
Gallbladder Leiomyoma GLL011
Gallbladder Leiomyosarcoma GLL016
Gallbladder Lipoma GLL003
Gallbladder Lymphoma GLL013
Gallbladder Melanoma GLL012
Gallbladder Mucinous Carcinoma GLL010
Gallbladder Neuroendocrine Tumor GLL034
Gallbladder Papillary Carcinoma GLL004
Gallbladder Papillomatosis GLL006
Gallbladder Pleomorphic Giant Cell Adenocarcinoma GLL005
Gallbladder Rhabdomyosarcoma GLL014
Gallbladder Sarcoma GLL021
Gallbladder Signet Ring Cell Adenocarcinoma GLL009
Gallbladder Small Cell Carcinoma GLL007
Gallbladder Squamous Cell Carcinoma GLL015
Gallbladder, Agenesis of GLL036
Galloway-Mowat Syndrome GLL032
Galloway-Mowat Syndrome 1 GLL038
Galloway-Mowat Syndrome 2 GLL043
Galloway-Mowat Syndrome 2, X-Linked GLL039
Galloway-Mowat Syndrome 3 GLL040
Galloway-Mowat Syndrome 4 GLL041
Galloway-Mowat Syndrome 5 GLL042
Gambling, Pathologic GMB002
Game Friedman Paradice Syndrome GMF001
Gamma Glutamyltransferase, Plasma Level of, Quantitative Trait Locus 1 GMM012
Gamma Glutamyltransferase, Plasma Level of, Quantitative Trait Locus 2 GMM013
Gamma Heavy Chain Disease GMM003
Gamma-a-Globulin, Defect in Assembly of GMM010
Gamma-Amino Butyric Acid Metabolism Disorder GMM004
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to GMM011
Gangliocytoma GNG005
Ganglioglioma GNG004
Ganglion or Cyst of Synovium/tendon/bursa GNG007
Ganglioneuroblastoma GNG008
Ganglioneuroma GNG002
Gangliosidosis Gm1 GNG001
Gangliosidosis Gm2 GNG010
Gapo Syndrome GPS001
Gardner-Diamond Syndrome GRD004
Garret Tripp Syndrome GRR001
Gars-Associated Axonal Neuropathy GRS004
Gas Bloat Syndrome GSB001
Gas Gangrene GSG001
Gasserian Ganglion Meningioma GSS001
Gastric Adenocarcinoma GST040
Gastric Adenocarcinoma and Proximal Polyposis of the Stomach GST086
Gastric Adenosquamous Carcinoma GST008
Gastric Antral Vascular Ectasia GST020
Gastric Body Carcinoma GST025
Gastric Cancer GST053
Gastric Cancer, Hereditary Diffuse GST103
Gastric Cardia Adenocarcinoma GST029
Gastric Cardia Carcinoma GST041
Gastric Diffuse Adenocarcinoma GST042
Gastric Dilatation GST007
Gastric Duplication Cysts GST055
Gastric Fundus Cancer GST026
Gastric Gastrinoma GST031
Gastric Hemangioma GST005
Gastric Juice Peptides GST104
Gastric Leiomyoma GST006
Gastric Leiomyosarcoma GST036
Gastric Linitis Plastica GST087
Gastric Liposarcoma GST011
Gastric Lymphoma GST027
Gastric Neuroendocrine Neoplasm GST004
Gastric Papillary Adenocarcinoma GST032
Gastric Pylorus Carcinoma GST022
Gastric Signet Ring Cell Adenocarcinoma GST016
Gastric Small Cell Carcinoma GST015
Gastric Sneezing GST101
Gastric Squamous Cell Carcinoma GST028
Gastric Teratoma GST043
Gastric Tubular Adenocarcinoma GST017
Gastric Ulcer GST023
Gastric Volvulus, Intrathoracic GST102
Gastrin Secretion Abnormality GST003
Gastrinoma GST030
Gastritis GST044
Gastritis, Familial Giant Hypertrophic GST095
Gastro-Enteropancreatic Neuroendocrine Tumor GST057
Gastrocutaneous Syndrome GST056
Gastroduodenal Crohn's Disease GST090
Gastroduodenitis GST039
Gastroenteritis GST045
Gastroesophageal Junction Adenocarcinoma GST012
Gastroesophageal Reflux GST092 GER
Gastrointestinal Adenoma GST038
Gastrointestinal Allergy GST078
Gastrointestinal Anthrax GST046
Gastrointestinal Carcinoma GST071
Gastrointestinal Defects and Immunodeficiency Syndrome GST093
Gastrointestinal Lymphoma GST014
Gastrointestinal Neuroendocrine Benign Tumor GST091
Gastrointestinal Neuroendocrine Tumor GST047
Gastrointestinal Stromal Tumor GST019
Gastrointestinal System Benign Neoplasm GST048
Gastrointestinal System Cancer GST049
Gastrointestinal System Disease GST050
Gastrointestinal Tuberculosis GST051
Gastrointestinal Tularemia GST018
Gastrojejunal Ulcer GST013
Gastroparesis GST037
Gastroschisis GST009
Gata1-Related X-Linked Cytopenia GT1001
Gatad2b-Associated Neurodevelopmental Disorder GTD002
Gaucher Disease - Ophthalmoplegia - Cardiovascular Calcification GCH019
Gaucher Disease, Atypical, Due to Saposin C Deficiency GCH010
Gaucher Disease, Perinatal Lethal GCH018
Gaucher Disease, Type I GCH015
Gaucher Disease, Type Ii GCH016
Gaucher Disease, Type Iii GCH017
Gaucher Disease, Type Iiic GCH013
Gaucher Ichthyosis Restrictive Dermopathy GCH007
Gaucher's Disease GCH001
Gay Feinmesser Cohen Syndrome GYF001
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 1 GZP003
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 2 GZP004
Gcgr-Related Hyperglucagonemia GCG001
Gdap1-Related Hereditary Motor and Sensory Neuropathy GDP003
Gelatinous Ascites GLT009
Geleophysic Dwarfism GLP002
Geleophysic Dysplasia GLP001
Geleophysic Dysplasia 1 GLP003
Geleophysic Dysplasia 2 GLP004
Geleophysic Dysplasia 3 GLP007
Gemignani Syndrome GMG001
Gemistocytic Astrocytoma GMS001
Gender Identity Disorder GND002
Gene Expression, Variation in, Quantitative Trait Locus on Chromosome 14 GNX002
Gene Expression, Variation in, Quantitative Trait Locus on Chromosome 20 GNX003
Generalized Anxiety Disorder GNR004
Generalized Atherosclerosis GNR003
Generalized Basal Epidermolysis Bullosa Simplex with Skin Atrophy, Scarring and Hair Loss GNR044
Generalized Epilepsy with Febrile Seizures Plus GNR002
Generalized Epilepsy with Febrile Seizures Plus, Type 1 GNR038
Generalized Epilepsy with Febrile Seizures Plus, Type 2 GNR039
Generalized Epilepsy with Febrile Seizures Plus, Type 3 GNR041
Generalized Epilepsy with Febrile Seizures Plus, Type 4 GNR040
Generalized Epilepsy with Febrile Seizures Plus, Type 6 GNR013
Generalized Epilepsy with Febrile Seizures Plus, Type 7 GNR043
Generalized Epilepsy with Febrile Seizures Plus, Type 8 GNR042
Generalized Epilepsy with Febrile Seizures Plus, Type 9 GNR034
Generalized Eruptive Histiocytosis GNR023
Generalized Eruptive Keratoacanthoma GNR033
Generalized Galactose Epimerase Deficiency GNR029
Generalized Gangliosidoses GNR012
Generalized Peeling Skin Syndrome GNR027
Generalized Resistance to Thyroid Hormone GNR008
Genetic Atypical Hemolytic-Uremic Syndrome GNT044
Genetic Epilepsy with Febrile Seizures Plus GNT046
Genetic Hyperferritinemia Without Iron Overload GNT037
Genetic Prion Diseases GNT033
Genetic Recurrent Myoglobinuria GNT042
Genetic Reflex Epilepsy GNT014
Genetic Transient Congenital Hypothyroidism GNT039
Geniculate Ganglionitis GNC005
Geniculate Herpes Zoster GNC003
Geniospasm 1 GNS004
Genital Dwarfism GNT015
Genital Dwarfism, Turner Type GNT016
Genital Herpes GNT003
Genitopalatocardiac Syndrome GNT043
Genitopatellar Syndrome GNT031
Genitourinary Tract Anomalies GNT050
Genochondromatosis GNC010
Genu Valgum, St. Helena Familial GNV002
Genuine Diffuse Phlebectasia GNN001
Geographic and Fissured Tongue GGR002
Geographic Tongue GGR001
Geotrichosis GTR001
Germ Cell and Embryonal Cancer GRM001
Germ Cells Tumors GRM010
German Syndrome GRM003
Geroderma Osteodysplastica GRD006
Geroderma Osteodysplasticum GRD005
Gershinibaruch Leibo Syndrome GRS005
Gerstmann Syndrome GRS001
Gerstmann-Straussler Disease GRS011
Gestational Choriocarcinoma GST052
Gestational Diabetes GST033
Gestational Diabetes Insipidus GST058
Gestational Ovarian Choriocarcinoma GST035
Gestational Trophoblastic Neoplasm GST010
Gestational Trophoblastic Tumor GST059
Gestational Uterine Corpus Choriocarcinoma GST021
Ghosal Hematodiaphyseal Dysplasia GHS005
Ghose Sachdev Kumar Syndrome GHS002
Giacheti Syndrome GCH021
Gianotti Crosti Syndrome GNT018
Giant Adenofibroma of the Breast GNT034
Giant Axonal Neuropathy GNT009
Giant Axonal Neuropathy 1, Autosomal Recessive GNT049
Giant Axonal Neuropathy 2 GNT045
Giant Axonal Neuropathy 2, Autosomal Dominant GNT040
Giant Cell Glioblastoma GNT002
Giant Cell Myocarditis GNT019
Giant Cell Reparative Granuloma GNT001
Giant Cell Tumor GNT008
Giant Congenital Nevus GNT020
Giant Ganglionic Hyperplasia GNT021
Giant Hemangioma GNT005
Giant Mammary Hamartoma GNT022
Giant Neutrophil Leukocytes GNT047
Giant Papillary Conjunctivitis GNT006
Giardiasis GRD001
Gigantiform Cementoma, Familial GGN006
Gigantism GGN002
Gigantism Advanced Bone Age Hoarse Cry GGN003
Gigantomastia GGN004
Gilbert Syndrome GLB001
Gilles De La Tourette Syndrome GLL008
Gillespie Syndrome GLL028
Gillessen-Kaesbach-Nishimura Syndrome GLL035
Gingival Disease GNG011
Gingival Fibromatosis GNG025
Gingival Hypertrophy GNG006
Gingival Overgrowth GNG012
Gingival Recession GNG003
Gingivitis GNG013
Gitelman Syndrome GTL001
Glanders GLN002
Glandular Cystitis GLN006
Glandular Pattern Ovarian Yolk Sac Tumor GLN004
Glandular Tularemia GLN001
Glandular-Alveolar Pattern Testicular Yolk Sac Tumor GLN005
Glans Penis Cancer GLN007
Glanzmann Thrombasthenia GLN010
Glass Syndrome GLS018
Glass-Chapman-Hockley Syndrome GLS019
Glassy Cell Carcinoma of the Cervix GLS012
Glassy Cell Carcinoma of the Cervix Uteri GLS017
Glassy Cell Variant Cervical Adenosquamous Carcinoma GLS005
Glaucoma 1, Open Angle, a GLC041
Glaucoma 1, Open Angle, B GLC101
Glaucoma 1, Open Angle, D GLC100
Glaucoma 1, Open Angle, F GLC078
Glaucoma 1, Open Angle, G GLC060
Glaucoma 1, Open Angle, H GLC076
Glaucoma 1, Open Angle, I GLC048
Glaucoma 1, Open Angle, J GLC102
Glaucoma 1, Open Angle, K GLC103
Glaucoma 1, Open Angle, M GLC051
Glaucoma 1, Open Angle, N GLC080
Glaucoma 1, Open Angle, O GLC104
Glaucoma 1, Open Angle, P GLC079
Glaucoma 1, Primary Open Angle, C GLC099
Glaucoma 3, Primary Congenital, a GLC097
Glaucoma 3, Primary Congenital, C GLC052
Glaucoma 3, Primary Congenital, D GLC054
Glaucoma 3, Primary Congenital, E GLC089
Glaucoma 3, Primary Infantile, B GLC083
Glaucoma and Sleep Apnea GLC088
Glaucoma Iridogoniodysgenesia GLC027
Glaucoma Type 1c GLC029
Glaucoma with Elevated Episcleral Venous Pressure GLC091
Glaucoma-Related Pigment Dispersion Syndrome GLC098
Glaucoma, Ectopia, Microspherophakia, Stiff Joints and Short Stature Syndrome GLC031
Glaucoma, Hereditary GLC032
Glaucoma, Hereditary Adult Type 1a GLC033
Glaucoma, Hereditary Juvenile Type 1b GLC034
Glaucoma, Normal Tension GLC084
Glaucoma, Primary Infantile Type 3a GLC035
Glaucoma, Primary Open Angle GLC092
Glaucomatocyclitic Crisis GLC001
Glaucomatous Atrophy of Optic Disc GLC005
Glb1-Related Disorders GLB016
Glioblastoma GLB002
Glioblastoma Classical Subtype GLB011
Glioblastoma Mesenchymal Subtype GLB013
Glioblastoma Multiforme GLB015
Glioblastoma Neural Subtype GLB014
Glioblastoma Proneural Subtype GLB012
Glioependymal/ependymal Cyst GLP005
Gliofibroma GLF001
Glioma GLM045
Glioma Susceptibility 1 GLM040
Glioma Susceptibility 2 GLM025
Glioma Susceptibility 3 GLM047
Glioma Susceptibility 4 GLM019
Glioma Susceptibility 5 GLM020
Glioma Susceptibility 6 GLM021
Glioma Susceptibility 7 GLM038
Glioma Susceptibility 8 GLM022
Glioma Susceptibility 9 GLM043
Gliomatosis Cerebri GLM004
Gliomatosis Peritonei GLM036
Gliosarcoma GLS001
Global Developmental Delay-Lung Cysts-Overgrowth-Wilms Tumor Syndrome GLB017
Global Developmental Delay-Osteopenia-Ectodermal Defect Syndrome GLB019
Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies GLB021
Global Disaccharide Intolerance GLB005
Globulin Anomaly Involving Beta -Globulin GLB023
Glomangioma GLM006
Glomangiomatosis GLM002
Glomangiomyoma GLM003
Glomangiosarcoma GLM005
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria GLM024
Glomeruloid Hemangioma GLM001
Glomerulonephritis GLM007
Glomerulopathy with Fibronectin Deposits 1 GLM014
Glomerulopathy with Fibronectin Deposits 2 GLM015
Glomus Tumor GLM008
Glomus Tympanicum Tumor GLM017
Glomus Vagale Tumor GLM046
Glomuvenous Malformations GLM012
Glossitis GLS007
Glossodynia GLS013
Glossopalatine Ankylosis GLS016
Glossopalatine Ankylosis Micrognathia Ear Anomalies GLS014
Glossopharyngeal Motor Neuropathy GLS006
Glossopharyngeal Nerve Disease GLS008
Glossopharyngeal Nerve Neoplasm GLS002
Glossopharyngeal Nerve Paralysis GLS003
Glossopharyngeal Neuralgia GLS004
Glottis Neoplasm GLT001
Glottis Squamous Cell Carcinoma GLT004
Glottis Verrucous Carcinoma GLT003
Glucagonoma GLC036
Glucocorticoid Deficiency 1 GLC042
Glucocorticoid Deficiency 2 GLC043
Glucocorticoid Deficiency 3 GLC053
Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency GLC105
Glucocorticoid Deficiency 5 GLC107
Glucocorticoid Resistance, Generalized GLC106
Glucocorticoid Therapy, Response to GLC077
Glucocorticoid-Induced Osteoporosis GLC086
Glucoglycinuria GLC094
Glucose Intolerance GLC003
Glucose Metabolism Disease GLC008
Glucose Phosphate Isomerase Deficiency GLC081
Glucose Transporter Type 1 Deficiency Syndrome GLC024
Glucose-6-Phosphate Translocase Deficiency GLC038
Glucose/galactose Malabsorption GLC022
Glucosephosphate Dehydrogenase Deficiency GLC009
Glucosephosphate Isomerase Deficiency GLC039
Glucosidase Acid-1,4-Alpha Deficiency GLC040
Glut1 Deficiency Syndrome 1 GLT018
Glut1 Deficiency Syndrome 2 GLT019
Glutamate Decarboxylase Deficiency GLT010
Glutamate Formiminotransferase Deficiency GLT005
Glutamic Acid Decarboxylase, Brain, Membrane Form GLT033
Glutamine Deficiency, Congenital GLT011
Glutamyl Ribose-5-Phosphate Storage Disease GLT038
Glutaric Acidemia I GLT035
Glutaric Acidemia Type Iii GLT029
Glutaric Aciduria Iii GLT028
Glutathione Peroxidase Deficiency GLT039
Glutathione Synthetase Deficiency GLT007
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due to GLT036
Glutathione Transferase Activity Toward Trans-Stilbene Oxide GLT034
Glutathionuria GLT014
Gluteal Muscles, Absence of GLT037
Gluten Allergy GLT030
Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency GLY022
Glycerol Kinase 2 GLY100
Glycerol Kinase 3 Pseudogene GLY101
Glycerol Kinase Deficiency GLY014
Glycerol Quantitative Trait Locus GLY102
Glycine Encephalopathy GLY010
Glycine Encephalopathy with Normal Serum Glycine GLY094
Glycine N-Methyltransferase Deficiency GLY015
Glycogen Storage Disease GLY013
Glycogen Storage Disease 0, Liver GLY058
Glycogen Storage Disease 0, Muscle GLY061
Glycogen Storage Disease Due to Acid Maltase Deficiency, Infantile Onset GLY052
Glycogen Storage Disease Due to Acid Maltase Deficiency, Late-Onset GLY074
Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency GLY081
Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency GLY078
Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency GLY085
Glycogen Storage Disease Due to Liver Phosphorylase Kinase Deficiency GLY065
Glycogen Storage Disease Ia GLY060
Glycogen Storage Disease Ib GLY016
Glycogen Storage Disease Ic GLY017
Glycogen Storage Disease Ii GLY008
Glycogen Storage Disease Iii GLY003
Glycogen Storage Disease Iv GLY007
Glycogen Storage Disease Ix GLY001
Glycogen Storage Disease Ixa GLY093
Glycogen Storage Disease Ixa1 GLY099
Glycogen Storage Disease Ixb GLY097
Glycogen Storage Disease Ixc GLY044
Glycogen Storage Disease of Heart, Lethal Congenital GLY033
Glycogen Storage Disease Type 0 GLY023
Glycogen Storage Disease V GLY004
Glycogen Storage Disease Vi GLY005
Glycogen Storage Disease Vii GLY011
Glycogen Storage Disease Viii GLY006
Glycogen Storage Disease X GLY057
Glycogen Storage Disease Xii GLY043
Glycogen Storage Disease Xiii GLY059
Glycogen Storage Disease Xv GLY009
Glycogen Storage Disease, Type Ixd GLY098
Glycogen-Rich Clear Cell Breast Carcinoma GLY012
Glycoprotein Storage Disease GLY096
Glycoprotein, Renal GLY095
Glycoproteinosis GLY031
Glycosylphosphatidylinositol Biosynthesis Defect 11 GLY106
Glycosylphosphatidylinositol Biosynthesis Defect 15 GLY103
Glycosylphosphatidylinositol Biosynthesis Defect 16 GLY104
Glycosylphosphatidylinositol Deficiency GLY032
Glyt1 Encephalopathy GLY105
Gm1-Gangliosidosis, Type I GM1004
Gm1-Gangliosidosis, Type Ii GM1005
Gm1-Gangliosidosis, Type Iii GM1006
Gm2 Gangliosidosis, 0 Variant GM2001
Gm2-Gangliosidosis, Ab Variant GM2005
Gm2-Gangliosidosis, B, B1, Ab Variant GM2002
Gmppa-Cdg GMP001
Gms Syndrome GMS002
Gnao1 Encephalopathy GN1001
Gnathodiaphyseal Dysplasia GNT026
Gnathomiasis GNT004
Gnathostoma Infection GNT023
Gne-Related Myopathy GNR020
Goat Milk Allergy GTM001
Goblet Cell Carcinoid GBL002
Goiter GTR002
Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors GTR011
Goiter, Multinodular 2 GTR013
Goiter, Multinodular 3 GTR014
Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies GTR012
Goldberg-Shprintzen Syndrome GLD006
Goldmann-Favre Syndrome GLD003
Gollop Coates Syndrome GLL023
Gombo Syndrome GMB001
Gomez-Lopez-Hernandez Syndrome GMZ002
Gonadal Agenesis GND011
Gonadal Disease GND003
Gonadal Dysgenesis GND004
Gonadal Dysgenesis, Xy Type, with Associated Anomalies GND012
Gonadoblastoma GND001
Gonococcal Bursitis GNC002
Gonococcal Endophthalmia GNC008
Gonococcal Iridocyclitis GNC004
Gonococcal Keratitis GNC007
Gonococcal Seminal Vesiculitis GNC009
Gonococcal Spondylitis GNC006
Gonococcal Synovitis GNC001
Good Syndrome GDS001
Goodpasture Syndrome GDP001
Gordon Holmes Syndrome GRD009
Gorham's Disease GRH001
Gorlin Bushkell Jensen Syndrome GRL001
Gosr2-Related Progressive Myoclonus Ataxia GSR001
Gout GT001
Gracile Bone Dysplasia GRC002
Gracile Syndrome GRC001
Grade Iii Astrocytoma GRD007
Graft-Versus-Host Disease GRF003
Graham Boyle Troxell Syndrome GRH002
Graham-Little-Piccardi-Lassueur Syndrome GRH005
Grand Kaine Fulling Syndrome GRN015
Granddad Syndrome GRN043
Grange Syndrome GRN034
Grant Syndrome GRN016
Granular Cell Leiomyosarcoma GRN012
Granular Cell Tumor GRN010
Granulocytopenia GRN017
Granulocytopenia with Immunoglobulin Abnormality GRN046
Granuloma Annulare GRN007
Granuloma Inguinale GRN005
Granulomas, Congenital Cerebral GRN018
Granulomatous Amebic Encephalitis GRN004
Granulomatous Angiitis GRN006
Granulomatous Dermatitis GRN003
Granulomatous Disease with Defect in Neutrophil Chemotaxis GRN047
Granulomatous Disease, Chronic, Autosomal Dominant Type GRN044
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative GRN048
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I GRN049
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii GRN050
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Iii GRN038
Granulomatous Disease, Chronic, X-Linked GRN051
Granulomatous Endometritis GRN001
Granulomatous Gastritis GRN011
Granulomatous Hepatitis GRN009
Granulomatous Hypophysitis GRN020
Granulomatous Lobular Mastitis GRN042
Granulomatous Mastitis GRN033
Granulomatous Myositis GRN036
Granulomatous Orchitis GRN002
Granulomatous Rosacea GRN021
Granulomatous Slack Skin Disease GRN032
Granulosa Cell Tumor of the Ovary GRN022
Granulosis Rubra Nasi GRN045
Graphite Pneumoconiosis GRP001
Graves Disease 1 GRV008
Graves Disease 2 GRV009
Graves Disease X-Linked 1 GRV013
Graves' Disease GRV001
Gray Platelet Syndrome GRY002
Gray Zone Lymphoma GRY001
Graying of Hair, Precocious GRY004
Grayson-Wilbrandt Corneal Dystrophy GRY003
Green Mud Crab Allergy GRN040
Green Sandford Davison Syndrome GRN023
Greenberg Dysplasia GRN013
Greig Cephalopolysyndactyly Syndrome GRG001
Grfoma GRF006
Grid2-Related Spinocerebellar Ataxia GRD008
Grin2a-Related Speech Disorders and Epilepsy GRN041
Grin2b Related Syndrome GRN053
Grin2b-Related Neurodevelopmental Disorder GRN052
Griscelli Syndrome GRS003
Griscelli Syndrome, Type 1 GRS013
Griscelli Syndrome, Type 2 GRS014
Griscelli Syndrome, Type 3 GRS012
Grix Blankenship Peterson Syndrome GRX001
Grn-Related Frontotemporal Dementia GRN014
Group B Strep Disease in Newborns GRP002
Grouped Pigmentation of the Retina GRP007
Grover's Disease GRV012
Growing Teratoma Syndrome GRW021
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia GRW037
Growth Factors, Combined Defect of GRW032
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy GRW038
Growth Hormone Deficiency GRW007
Growth Hormone Deficiency, Isolated Partial GRW023
Growth Hormone Insensitivity with Immunodeficiency GRW003
Growth Hormone Insensitivity, Partial GRW026
Growth Hormone Secreting Pituitary Adenoma GRW001
Growth Restriction, Severe, with Distinctive Facies GRW027
Growth Retardation Alopecia Pseudoanodontia Optic GRW009
Growth Retardation Hydrocephaly Lung Hypoplasia GRW010
Growth Retardation-Mild Developmental Delay-Chronic Hepatitis Syndrome GRW022
Growth Retardation, Deafness, Femoral Epiphyseal Dysplasia, and Lacrimal Duct Obstruction GRW034
Growth Retardation, Developmental Delay, and Facial Dysmorphism GRW039
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, and Hepatopathy GRW035
Growth Retardation, Small and Puffy Hands and Feet, and Eczema GRW033
Grubben De Cock Borghgraef Syndrome GRB001
Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia GTP002
Guanylate Cyclase 2e, Pseudogene GNY003
Guanylate Kinase 3 GNY002
Guillain-Barre Syndrome GLL022
Guillain-Barre Syndrome, Familial GLL037
Guizar Vasquez Sanchez Manzano Syndrome GZR001
Gum Cancer GMC001
Gummatous Syphilis GMM001
Gupta Patton Syndrome GPT001
Gurrieri Syndrome GRR002
Guttate Psoriasis GTT002
Gynandroblastoma GYN003
Gynatresia GYN002
Gynecomastia GYN001
Gyrate Atrophy of Choroid and Retina GYR004
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