Disease Name Symbol Acronym
G6pc3 Deficiency G6P001
Gaba Aminotransferase Deficiency GBM001 ABAT
Gaba-Transaminase Deficiency GBT001 GABATD
Gabriele-De Vries Syndrome GBR007 GADEVS
Gait Apraxia GTP001
Gait Ataxia with Late Onset Polyneuropathy Syndrome GTT003
Galactokinase Deficiency GLC004 GALCT2
Galactorrhea GLC096
Galactorrhoea-Hyperprolactinaemia GLC025
Galactose Epimerase Deficiency GLC011 EDG
Galactosemia GLC006 GALCT
Galactosialidosis GLC012 GSL
Gall Bladder Carcinoma in Situ GLL001
Gallamine Allergy GLL044
Gallbladder Adenocarcinoma GLL017
Gallbladder Adenoma GLL029
Gallbladder Angiosarcoma GLL002
Gallbladder Cancer GLL018
Gallbladder Disease GLL020
Gallbladder Disease 1 GLL024 GBD1
Gallbladder Disease 2 GLL025 GBD2
Gallbladder Disease 3 GLL026 GBD3
Gallbladder Disease 4 GLL027 GBD4
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 GAMOS1
Galloway-Mowat Syndrome 2 GLL043
Galloway-Mowat Syndrome 2, X-Linked GLL039 GAMOS2
Galloway-Mowat Syndrome 3 GLL040 GAMOS3
Galloway-Mowat Syndrome 4 GLL041 GAMOS4
Galloway-Mowat Syndrome 5 GLL042 GAMOS5
Galloway-Mowat Syndrome 6 GLL045 GAMOS6
Galloway-Mowat Syndrome 7 GLL046 GAMOS7
Galloway-Mowat Syndrome 8 GLL047 GAMOS8
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 HAGGSD
Gangliocytoma GNG005
Ganglioglioma GNG004
Ganglion or Cyst of Synovium/tendon/bursa GNG007
Ganglioneuroblastoma GNG008
Ganglioneuroma GNG002
Gangliosidosis GNG009
Gapo Syndrome GPS001 GAPOS
Gardner-Diamond Syndrome GRD004 GDS
Garret Tripp Syndrome GRR001
Gars1-Associated Axonal Neuropathy GRS015
Gas Bloat Syndrome GSB001
Gas Gangrene GSG001
Gasserian Ganglion Meningioma GSS001
Gastric Adenocarcinoma GST040
Gastric Adenocarcinoma and Proximal Polyposis of the Stomach GST086 GAPPS
Gastric Adenosquamous Carcinoma GST008
Gastric Antral Vascular Ectasia GST020 GAVE
Gastric Body Carcinoma GST025
Gastric Cancer GST053 GASC
Gastric Cancer, Hereditary Diffuse GST103 HDGC
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 GNET
Gastric Non-Hodgkin Lymphoma GST107
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
Gastrocutaneous Syndrome GST056
Gastroduodenal Crohn's Disease GST090
Gastroduodenal Malformation GST110
Gastroduodenitis GST039
Gastroenteric Neuroendocrine Neoplasm GST109
Gastroenteritis GST045
Gastroenteropancreatic Neuroendocrine Neoplasm GST111
Gastro-Enteropancreatic Neuroendocrine Tumor GST057
Gastroesophageal Adenocarcinoma GST105
Gastroesophageal Junction Adenocarcinoma GST012
Gastroesophageal Reflux GST092 GER
Gastrointestinal Adenoma GST038
Gastrointestinal Anthrax GST046
Gastrointestinal Carcinoma GST071
Gastrointestinal Defects and Immunodeficiency Syndrome GST093 GIDID
Gastrointestinal Lymphoma GST014
Gastrointestinal Neuroendocrine Benign Tumor GST091
Gastrointestinal Neuroendocrine Tumor GST047
Gastrointestinal Stromal Tumor GST019 GIST
Gastrointestinal System Benign Neoplasm GST048
Gastrointestinal System Cancer GST049
Gastrointestinal System Disease GST050
Gastrointestinal Tuberculosis GST051
Gastrointestinal Tularemia GST018
Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets GST106 GURDP
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 AGD
Gaucher Disease, Perinatal Lethal GCH018 GDPL
Gaucher Disease, Type I GCH015 GD
Gaucher Disease, Type Ii GCH016 GD2
Gaucher Disease, Type Iii GCH017 GD3
Gaucher Disease, Type Iiic GCH013 GD3C
Gaucher Ichthyosis Restrictive Dermopathy GCH007
Gaucher's Disease GCH001 GD
Gay Feinmesser Cohen Syndrome GYF001
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 GZP005 HGPPS1
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 2, with Impaired Intellectual Development GZP006 HGPPS2
Gcgr-Related Hyperglucagonemia GCG001
Gdap1-Related Hereditary Motor and Sensory Neuropathy GDP003
Geleophysic Dwarfism GLP002
Geleophysic Dysplasia GLP001
Geleophysic Dysplasia 1 GLP003 GPHYSD1
Geleophysic Dysplasia 2 GLP004 GPHYSD2
Geleophysic Dysplasia 3 GLP007 GPHYSD3
Gemignani Syndrome GMG001
Gemistocytic Astrocytoma GMS001
Gender Identity Disorder GND002
Gene Expression, Variation in, Quantitative Trait Locus on Chromosome 14 GNX002 GEVQ1
Gene Expression, Variation in, Quantitative Trait Locus on Chromosome 20 GNX003 GEVQ2
Generalized Anxiety Disorder GNR004
Generalized Atherosclerosis GNR003
Generalized Bulbospinal Muscular Atrophy GNR047
Generalized Epilepsy with Febrile Seizures Plus GNR002 GEFS+
Generalized Epilepsy with Febrile Seizures Plus, Type 1 GNR038 GEFSP1
Generalized Epilepsy with Febrile Seizures Plus, Type 10 GNR046 GEFSP10
Generalized Epilepsy with Febrile Seizures Plus, Type 2 GNR039 GEFSP2
Generalized Epilepsy with Febrile Seizures Plus, Type 4 GNR040 GEFSP4
Generalized Epilepsy with Febrile Seizures Plus, Type 6 GNR013 GEFSP6
Generalized Epilepsy with Febrile Seizures Plus, Type 7 GNR043 GEFSP7
Generalized Epilepsy with Febrile Seizures Plus, Type 8 GNR042 GEFSP8
Generalized Epilepsy with Febrile Seizures Plus, Type 9 GNR034 GEFSP9
Generalized Eruptive Histiocytosis GNR023
Generalized Eruptive Keratoacanthoma GNR033 GEKA
Generalized Galactose Epimerase Deficiency GNR029
Generalized Gangliosidoses GNR012
Generalized Isolated Dystonia GNR048
Generalized Juvenile Polyposis/juvenile Polyposis Coli GNR035
Generalized Lipodystrophy-Associated Progeroid Syndrome GNR045
Generalized Peeling Skin Syndrome GNR027
Generalized Resistance to Thyroid Hormone GNR008 GRTH
Genetic 46,xx Disorder of Sex Development GNT132
Genetic 46,xy Disorder of Sex Development GNT135
Genetic 46,xy Disorder of Sex Development of Endocrine Origin GNT134
Genetic Acrokeratoderma GNT097
Genetic Alopecia GNT163
Genetic Atypical Hemolytic-Uremic Syndrome GNT044
Genetic Biliary Tract Disease GNT103
Genetic Bone Tumor GNT079
Genetic Branchial Arch or Oral-Acral Syndrome GNT065
Genetic Cardiac Anomaly GNT114
Genetic Cardiac Malformation GNT164
Genetic Cardiac Rhythm Disease GNT177
Genetic Cardiac Tumor GNT111
Genetic Central Nervous System and Retinal Vascular Disease GNT080
Genetic Central Nervous System Malformation GNT081
Genetic Cerebellar Malformation GNT123
Genetic Cerebral Malformation GNT121
Genetic Cerebral Small Vessel Disease GNT165
Genetic Chronic Primary Adrenal Insufficiency GNT178
Genetic Complex Vascular Malformation with Associated Anomalies GNT146
Genetic Congenital Limb Malformation GNT077
Genetic Congenital Malformation of the Eye with Glaucoma As a Major Feature GNT168
Genetic Corneal Dystrophy GNT169
Genetic Cranial Malformation GNT075
Genetic Dementia GNT105
Genetic Dermis Disorder GNT090
Genetic Dermis Elastic Tissue Disorder GNT129
Genetic Developmental Defect of the Eye GNT069
Genetic Digestive Tract Malformation GNT074
Genetic Digestive Tract Tumor GNT113
Genetic Disorder of Sex Development GNT133
Genetic Disorder of Sex Development of Gynecological Interest GNT136
Genetic Endocrine Growth Disease GNT101
Genetic Epidermal Appendage Anomaly GNT098
Genetic Epidermal Disorder GNT100
Genetic Epilepsy with Febrile Seizures Plus GNT046 GEFS+
Genetic Erythrokeratoderma GNT095
Genetic Eye Tumor GNT060
Genetic Facial Cleft GNT160
Genetic Frontotemporal Degeneration with Dementia GNT109
Genetic Gastro-Esophageal Disease GNT053
Genetic Glomerular Disease GNT068
Genetic Gynecological Tumor GNT056
Genetic Hair Anomaly GNT035
Genetic Head and Neck Malformation GNT067
Genetic Hemoglobinopathy GNT148
Genetic Hyperaldosteronism GNT152
Genetic Hyperferritinemia Without Iron Overload GNT037
Genetic Hyperparathyroidism GNT127
Genetic Hyperpigmentation of the Skin GNT091
Genetic Hypertension GNT029
Genetic Hypoparathyroidism GNT126
Genetic Hypopigmentation of the Skin GNT092
Genetic Immune Deficiency with Skin Involvement GNT085
Genetic Infertility GNT108
Genetic Inflammatory or Rheumatoid-Like Osteoarthropathy GNT161
Genetic Interstitial Lung Disease GNT107
Genetic Intestinal Disease GNT054
Genetic Intestinal Disease Due to Fat Malabsorption GNT140
Genetic Intestinal Polyposis GNT138
Genetic Intractable Diarrhea of Infancy GNT139 IDI
Genetic Larynx Anomaly GNT156
Genetic Lens and Zonula Anomaly GNT061
Genetic Lethal Multiple Congenital Anomalies/dysmorphic Syndrome GNT166
Genetic Lipodystrophy GNT041
Genetic Malformation Syndrome with Odontal and/or Periodontal Component GNT066
Genetic Malformation Syndrome with Short Stature GNT070
Genetic Mixed Dermis Disorder GNT089
Genetic Motor Neuron Disease GNT176
Genetic Multiple Congenital Anomalies/dysmorphic Syndrome GNT078
Genetic Multiple Congenital Anomalies/dysmorphic Syndrome Without Intellectual Disability GNT130
Genetic Multiple Congenital Anomalies/dysmorphic Syndrome-Variable Intellectual Disability Syndrome GNT131
Genetic Nail Anomaly GNT099
Genetic Neurodegenerative Disease GNT083
Genetic Neurodegenerative Disease with Dementia GNT110
Genetic Neuroendocrine Tumor GNT115
Genetic Neurological Channelopathy of the Central Nervous System GNT173
Genetic Neurological Muscular Channelopathy GNT172
Genetic Neuromuscular Disease GNT082
Genetic Neuromuscular Junction Disease GNT175
Genetic Neuro-Ophthalmological Disease GNT058
Genetic Neurovascular Malformation GNT153
Genetic Non-Acquired Premature Ovarian Failure GNT162
Genetic Non-Syndromic Central Nervous System Malformation GNT120
Genetic Non-Syndromic Obesity GNT051
Genetic Non-Syndromic Renal or Urinary Tract Malformation GNT143
Genetic Nose and Cavum Anomaly GNT157
Genetic Obesity GNT167
Genetic Otorhinolaryngologic Disease GNT147
Genetic Otorhinolaryngological Malformation GNT158
Genetic Overgrowth/obesity Syndrome GNT071
Genetic Pancreatic Disease GNT052
Genetic Parenchymatous Liver Disease GNT104
Genetic Peripheral Neuropathy GNT174
Genetic Photodermatosis GNT084
Genetic Pigmentation Anomaly of the Skin GNT094
Genetic Polycythemia GNT106
Genetic Polyendocrinopathy GNT057
Genetic Porokeratosis GNT096
Genetic Posterior Fossa Malformation GNT122
Genetic Precocious Puberty GNT155
Genetic Precocious Puberty in Female GNT154
Genetic Primary Lymphedema GNT145
Genetic Primary Orthostatic Disorder GNT171
Genetic Primary Orthostatic Hypotension GNT144
Genetic Prion Diseases GNT033 TSES
Genetic Progeroid Syndrome GNT142
Genetic Recurrent Myoglobinuria GNT042
Genetic Reflex Epilepsy GNT014
Genetic Renal or Urinary Tract Malformation GNT076
Genetic Renal Tubular Disease GNT063
Genetic Renal Tumor GNT064
Genetic Respiratory Malformation GNT059
Genetic Respiratory or Mediastinal Malformation GNT072
Genetic Sebaceous Gland Anomaly GNT093
Genetic Skeletal Muscle Disease GNT125
Genetic Skin Tumor GNT087
Genetic Skin Vascular Disorder GNT088
Genetic Soft Tissue Tumor GNT112
Genetic Subcutaneous Tissue Disorder GNT086
Genetic Superficial Corneal Dystrophy GNT170
Genetic Susceptibility to Infections Due to Particular Pathogens GNT055
Genetic Syndrome with a Central Nervous System Malformation As Major Feature GNT124
Genetic Syndrome with a Cerebellar Malformation As Major Feature GNT117
Genetic Syndrome with a Dandy-Walker Malformation As Major Feature GNT118
Genetic Syndrome with Corpus Callosum Agenesis/dysgenesis As a Major Feature GNT119
Genetic Syndrome with Limb Malformations As a Major Feature GNT149
Genetic Syndrome with Limb Reduction Defects GNT150
Genetic Syndromic Esophageal Malformation GNT151
Genetic Syndromic Pierre Robin Syndrome GNT141
Genetic Thrombotic Microangiopathy GNT062
Genetic Tracheal Anomaly GNT159
Genetic Transient Congenital Hypothyroidism GNT039
Genetic Tumor of Hematopoietic and Lymphoid Tissues GNT137
Genetic Urogenital Tract Malformation GNT102
Genetic Urogenital Tumor GNT116
Genetic Urticaria GNT036
Genetic Vascular Anomaly GNT128
Genetic Visceral Malformation of the Liver, Biliary Tract, Pancreas or Spleen GNT073
Geniculate Ganglionitis GNC005
Geniculate Herpes Zoster GNC003
Geniospasm 1 GNS004 GSM1
Genital Dwarfism GNT015
Genital Dwarfism, Turner Type GNT016
Genital Herpes GNT003
Genitopalatocardiac Syndrome GNT043
Genitopatellar Syndrome GNT031 GTPTS
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 Cell Cancer GRM005
Germ Cells Tumors GRM010
German Syndrome GRM003
Germinoma GRM004
Geroderma Osteodysplasticum GRD005 GO
Gershinibaruch Leibo Syndrome GRS005
Gerstmann Syndrome GRS001 GS
Gerstmann-Straussler Disease GRS011 GSD
Gestational Choriocarcinoma GST052
Gestational Diabetes GST033 GDM
Gestational Diabetes Insipidus GST058
Gestational Ovarian Choriocarcinoma GST035
Gestational Trophoblastic Neoplasm GST010 GTN
Gestational Trophoblastic Tumor GST059 GTN
Gestational Uterine Corpus Choriocarcinoma GST021
Ghosal Hematodiaphyseal Dysplasia GHS005 GHDD
Ghose Sachdev Kumar Syndrome GHS002
Giacheti Syndrome GCH021
Gianotti Crosti Syndrome GNT018 GCS
Giant Adenofibroma of the Breast GNT034
Giant Axonal Neuropathy GNT009 GAN
Giant Axonal Neuropathy 1, Autosomal Recessive GNT049 GAN1
Giant Axonal Neuropathy 2 GNT045
Giant Axonal Neuropathy 2, Autosomal Dominant GNT040 GAN2
Giant Cell Glioblastoma GNT002
Giant Cell Myocarditis GNT019 GCM
Giant Cell Reparative Granuloma GNT001
Giant Cell Tumor GNT008
Giant Congenital Nevus GNT020 GMN
Giant Hemangioma GNT005
Giant Mammary Hamartoma GNT022
Giant Neutrophil Leukocytes GNT047
Giant Papillary Conjunctivitis GNT006 GPC
Giardiasis GRD001
Gigantiform Cementoma, Familial GGN006
Gigantism GGN002
Gigantism Advanced Bone Age Hoarse Cry GGN003
Gigantomastia GGN004
Gilbert Syndrome GLB001 GILBS
Gilles De La Tourette Syndrome GLL008 GTS
Gillespie Syndrome GLL028 GLSP
Gillessen-Kaesbach-Nishimura Syndrome GLL035 GIKANIS
Gingival Disease GNG011
Gingival Fibromatosis GNG025
Gingival Hypertrophy GNG006
Gingival Overgrowth GNG012
Gingival Recession GNG003
Gingivitis GNG013
Gist-Plus Syndrome GST108 GISTPS
Gitelman Syndrome GTL001 GTLMNS
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 GT
Glass Syndrome GLS018 GLASS
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 GLC1A
Glaucoma 1, Open Angle, B GLC101 GLC1B
Glaucoma 1, Open Angle, D GLC100 GLC1D
Glaucoma 1, Open Angle, F GLC078 GLC1F
Glaucoma 1, Open Angle, G GLC060 GLC1G
Glaucoma 1, Open Angle, H GLC076 GLC1H
Glaucoma 1, Open Angle, I GLC048 GLC1I
Glaucoma 1, Open Angle, J GLC102 GLC1J
Glaucoma 1, Open Angle, K GLC103 GLC1K
Glaucoma 1, Open Angle, M GLC051 GLC1M
Glaucoma 1, Open Angle, N GLC080 GLC1N
Glaucoma 1, Open Angle, O GLC104 GLC1O
Glaucoma 1, Open Angle, P GLC079 GLC1P
Glaucoma 1, Primary Open Angle, C GLC099 GLC1C
Glaucoma 3, Primary Congenital, a GLC097 GLC3A
Glaucoma 3, Primary Congenital, C GLC052 GLC3C
Glaucoma 3, Primary Congenital, D GLC054 GLC3D
Glaucoma 3, Primary Congenital, E GLC089 GLC3E
Glaucoma 3, Primary Infantile, B GLC083 GLC3B
Glaucoma and Sleep Apnea GLC088
Glaucoma Iridogoniodysgenesia GLC027
Glaucoma Type 1c GLC029
Glaucoma with Elevated Episcleral Venous Pressure GLC091
Glaucoma, Ectopia, Microspherophakia, Stiff Joints and Short Stature Syndrome GLC031 GEMSS
Glaucoma, Hereditary GLC032
Glaucoma, Hereditary Adult Type 1a GLC033
Glaucoma, Hereditary Juvenile Type 1b GLC034
Glaucoma, Normal Tension GLC084 NPG
Glaucoma, Primary Infantile Type 3a GLC035
Glaucoma, Primary Open Angle GLC092 POAG
Glaucoma-Related Pigment Dispersion Syndrome GLC098 GPDS1
Glaucomatocyclitic Crisis GLC001
Glaucomatous Atrophy of Optic Disc GLC005
Glb1-Related Disorders GLB016
Glial Tumor GLL048
Glial Tumor of Neuroepithelial Tissue with Unknown Origin GLL049
Glioblastoma GLB002 GBM
Glioblastoma Classical Subtype GLB011
Glioblastoma Mesenchymal Subtype GLB013
Glioblastoma Multiforme GLB015 GBM
Glioblastoma Neural Subtype GLB014
Glioblastoma Proneural Subtype GLB012
Glioependymal/ependymal Cyst GLP005
Gliofibroma GLF001
Glioma GLM045
Glioma Susceptibility 1 GLM040 GLM1
Glioma Susceptibility 2 GLM025 GLM2
Glioma Susceptibility 3 GLM047 GLM3
Glioma Susceptibility 4 GLM019 GLM4
Glioma Susceptibility 5 GLM020 GLM5
Glioma Susceptibility 6 GLM021 GLM6
Glioma Susceptibility 7 GLM038 GLM7
Glioma Susceptibility 8 GLM022 GLM8
Glioma Susceptibility 9 GLM043 GLM9
Gliomatosis Cerebri GLM004
Gliomatosis Peritonei GLM036
Gliosarcoma GLS001
Global Cerebellar Malformation GLB027
Global Developmental Delay with or Without Impaired Intellectual Development GLB025 GDDI
Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies GLB021 GDACCF
Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor GLB024 GLOW
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine GLB026 GDPAG
Global Developmental Delay-Alopecia-Macrocephaly-Facial Dysmorphism-Structural Brain Anomalies Syndrome GLB028
Global Developmental Delay-Osteopenia-Ectodermal Defect Syndrome GLB019
Global Disaccharide Intolerance GLB005
Globulin Anomaly Involving Beta -Globulin GLB023
Glomangioma GLM006
Glomangiomatosis GLM002
Glomangiomyoma GLM003
Glomangiosarcoma GLM005
Glomerular Disease GLM044
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria GLM024 GCKDHI
Glomeruloid Hemangioma GLM001
Glomerulonephritis GLM007
Glomerulopathy with Fibronectin Deposits 1 GLM014 GFND1
Glomerulopathy with Fibronectin Deposits 2 GLM015 GFND2
Glomus Tumor GLM008
Glomus Tympanicum Tumor GLM017
Glomus Vagale Tumor GLM046
Glomuvenous Malformations GLM012 GVM
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 GCCD1
Glucocorticoid Deficiency 2 GLC043 GCCD2
Glucocorticoid Deficiency 3 GLC053 GCCD3
Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency GLC105 GCCD4
Glucocorticoid Deficiency 5 GLC107 GCCD5
Glucocorticoid Resistance, Generalized GLC106 GCCR
Glucocorticoid Therapy, Response to GLC077 GCTR
Glucocorticoid-Induced Osteoporosis GLC086
Glucoglycinuria GLC094
Gluconeogenesis Disorder GLC108
Glucose Intolerance GLC003
Glucose Metabolism Disease GLC008
Glucose Phosphate Isomerase Deficiency GLC081
Glucose Transport Disorder GLC109
Glucose Transporter Type 1 Deficiency Syndrome GLC024 GTPS
Glucose/galactose Malabsorption GLC022 GGM
Glucose-6-Phosphate Translocase Deficiency GLC038
Glucosephosphate Dehydrogenase Deficiency GLC009
Glucosephosphate Isomerase Deficiency GLC039
Glucosidase Acid-1,4-Alpha Deficiency GLC040
Glut1 Deficiency Syndrome 1 GLT018 GLUT1DS1
Glut1 Deficiency Syndrome 2 GLT019 GLUT1DS2
Glutamate Decarboxylase Deficiency GLT010
Glutamate Formiminotransferase Deficiency GLT005 FIGLU-URIA
Glutamic Acid Decarboxylase, Brain, Membrane Form GLT033
Glutamine Deficiency, Congenital GLT011 CSGD
Glutamyl Ribose-5-Phosphate Storage Disease GLT038
Glutaric Acidemia I GLT035 GA1
Glutaric Acidemia Type Iii GLT029
Glutaric Aciduria Iii GLT028 GA3
Glutathione Peroxidase Deficiency GLT039 GPXD
Glutathione Synthetase Deficiency GLT007 GSSD
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due to GLT036 GSSDE
Glutathione Transferase Activity Toward Trans-Stilbene Oxide GLT034
Glutathionuria GLT014 GLUTH
Gluteal Muscles, Absence of GLT037
Gluten Allergy GLT030
Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency GLY022
Glycerol Kinase 2 GLY100 GK2
Glycerol Kinase 3 Pseudogene GLY101 GK3P
Glycerol Kinase Deficiency GLY014 GKD
Glycerol Quantitative Trait Locus GLY102 GLYCQTL
Glycine Encephalopathy GLY010 GCE
Glycine Encephalopathy with Normal Serum Glycine GLY094 GCENSG
Glycine N-Methyltransferase Deficiency GLY015 GNMT DEFICIENCY
Glycogen Storage Disease GLY013 GSD
Glycogen Storage Disease 0, Liver GLY058 GSD0A
Glycogen Storage Disease 0, Muscle GLY061 GSD0B
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 Glucose-6-Phosphatase Deficiency Type Ib GLY111 GSDIB
Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency GLY078
Glycogen Storage Disease Due to Glycogen Synthase Deficiency GLY110
Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency GLY085
Glycogen Storage Disease Due to Liver Phosphorylase Kinase Deficiency GLY065 XLG
Glycogen Storage Disease Due to Phosphorylase Kinase Deficiency GLY054
Glycogen Storage Disease Ia GLY060 GSD1A
Glycogen Storage Disease Ib GLY016 GSD1B
Glycogen Storage Disease Ic GLY017 GSD1C
Glycogen Storage Disease Ii GLY008 GSD2
Glycogen Storage Disease Iii GLY003 GSD3
Glycogen Storage Disease Iv GLY007 GSD4
Glycogen Storage Disease Ix GLY001
Glycogen Storage Disease Ixa GLY093
Glycogen Storage Disease Ixa1 GLY099 GSD9A1
Glycogen Storage Disease Ixb GLY097 GSD9B
Glycogen Storage Disease Ixc GLY044 GSD9C
Glycogen Storage Disease of Heart, Lethal Congenital GLY033 GSDH
Glycogen Storage Disease Type 0 GLY023 GSD 0
Glycogen Storage Disease V GLY004 GSD5
Glycogen Storage Disease Vi GLY005 GSD6
Glycogen Storage Disease Vii GLY011 GSD7
Glycogen Storage Disease Viii GLY006 PYKL
Glycogen Storage Disease with Hypertrophic Cardiomyopathy GLY109
Glycogen Storage Disease X GLY057 GSD10
Glycogen Storage Disease Xii GLY043 GSD12
Glycogen Storage Disease Xiii GLY059 GSD13
Glycogen Storage Disease Xv GLY009 GSD15
Glycogen Storage Disease, Type Ixd GLY098 GSD9D
Glycogen-Rich Clear Cell Breast Carcinoma GLY012
Glycoprotein Storage Disease GLY096
Glycoprotein, Renal GLY095
Glycoproteinosis GLY031
Glycosylphosphatidylinositol Biosynthesis Defect 11 GLY106 GPIBD11
Glycosylphosphatidylinositol Biosynthesis Defect 15 GLY103 GPIBD15
Glycosylphosphatidylinositol Biosynthesis Defect 16 GLY104 GPIBD16
Glycosylphosphatidylinositol Biosynthesis Defect 17 GLY107 GPIBD17
Glycosylphosphatidylinositol Biosynthesis Defect 18 GLY108 GPIBD18
Glycosylphosphatidylinositol Deficiency GLY032 GPID
Glyt1 Encephalopathy GLY105
Gm1 Gangliosidosis GM1007
Gm1-Gangliosidosis, Type I GM1004 GM1G1
Gm1-Gangliosidosis, Type Ii GM1005 GM1G2
Gm1-Gangliosidosis, Type Iii GM1006 GM1G3
Gm2 Gangliosidosis GM2006
Gm2 Gangliosidosis, 0 Variant GM2001
Gm2-Gangliosidosis, Ab Variant GM2005 GM2GAB
Gm2-Gangliosidosis, B, B1, Ab Variant GM2002
Gmppa-Cdg GMP001
Gms Syndrome GMS002
Gnao1 Encephalopathy GN1001
Gnathodiaphyseal Dysplasia GNT026 GDD
Gnathomiasis GNT004
Gnathostoma Infection GNT023
Gne-Related Myopathy GNR020 DMRV
Goat Milk Allergy GTM001
Goblet Cell Carcinoid GBL002 GCC
Goiter GTR002
Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors GTR011 MNG1
Goiter, Multinodular 2 GTR013 MNG2
Goiter, Multinodular 3 GTR014 MNG3
Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies GTR012
Goldberg-Shprintzen Syndrome GLD006 GOSHS
Goldmann-Favre Syndrome GLD003
Gollop Coates Syndrome GLL023
Gombo Syndrome GMB001
Gomez-Lopez-Hernandez Syndrome GMZ002 GLHS
Gonadal Agenesis GND011
Gonadal Disease GND003
Gonadal Dysgenesis GND004
Gonadal Dysgenesis of Gynecological Interest GND016
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy, and Myopathy GND014 GDRM
Gonadal Dysgenesis, Xy Type, with Associated Anomalies GND012
Gonadal Germ Cell Tumor GND015
Gonadoblastoma GND001 GBY
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 GDHS
Gorham's Disease GRH001
Gosr2-Related Progressive Myoclonus Ataxia GSR001 EPM6
Gout GT001 GOUT
Gracile Bone Dysplasia GRC002 GCLEB
Gracile Syndrome GRC001 GRACILE
Grade Iii Astrocytoma GRD007
Graft-Versus-Host Disease GRF003 GVHDS
Graham Boyle Troxell Syndrome GRH002
Graham-Little-Piccardi-Lassueur Syndrome GRH005
Grand Kaine Fulling Syndrome GRN015
Granddad Syndrome GRN043
Grange Syndrome GRN034 GRNG
Grant Syndrome GRN016
Granular Cell Carcinoma GRN008
Granular Cell Leiomyosarcoma GRN012
Granular Cell Tumor GRN010
Granular Corneal Dystrophy GRN055
Granulocytopenia GRN017
Granuloma Annulare GRN007
Granuloma Inguinale GRN005
Granulomas, Congenital Cerebral GRN018
Granulomatosis with Polyangiitis GRN037 GPA
Granulomatous Amebic Encephalitis GRN004
Granulomatous Angiitis GRN006
Granulomatous Autoinflammatory Syndrome GRN058
Granulomatous Autoinflammatory Syndrome of Childhood GRN057
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 ARCGD
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I GRN049 CDG1
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii GRN050 CDG2
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Iii GRN038 CDG3
Granulomatous Disease, Chronic, X-Linked GRN051 CDGX
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 GTCT
Granulosis Rubra Nasi GRN045
Graphite Pneumoconiosis GRP001
Graves' Disease GRV001
Graves Disease 1 GRV008 GRD1
Graves Disease 2 GRV009 GRD2
Graves Disease X-Linked 1 GRV013 GRDX1
Gray Platelet Syndrome GRY002 GPS
Gray Zone Lymphoma GRY001
Graying of Hair, Precocious GRY004
Grayson-Wilbrandt Corneal Dystrophy GRY003 GWCD
Green Sandford Davison Syndrome GRN023
Greenberg Dysplasia GRN013 GRBGD
Greig Cephalopolysyndactyly Syndrome GRG001 GCPS
Grfoma GRF006
Grid2-Related Spinocerebellar Ataxia GRD008
Grin1-Associated Disorders GRN054
Grin1-Related Neurodevelopmental Disorder GRN056
Grin2a-Related Speech Disorders and Epilepsy GRN041
Grin2b Related Syndrome GRN053
Grin2b-Related Neurodevelopmental Disorder GRN052
Griscelli Syndrome GRS003 GS
Griscelli Syndrome, Type 1 GRS013 GS1
Griscelli Syndrome, Type 2 GRS014 GS2
Griscelli Syndrome, Type 3 GRS012 GS3
Grix Blankenship Peterson Syndrome GRX001
Grn-Related Frontotemporal Dementia GRN014 FTLD
Group B Strep Disease in Newborns GRP002
Grouped Pigmentation of the Retina GRP007
Grover's Disease GRV012 TAD
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 GHDP
Growth Hormone Insensitivity with Immunodeficiency GRW003 GHII
Growth Hormone Insensitivity, Partial GRW026 GHIP
Growth Hormone Secreting Pituitary Adenoma GRW001
Growth Restriction, Severe, with Distinctive Facies GRW027 GRDF
Growth Retardation Hydrocephaly Lung Hypoplasia GRW010
Growth Retardation, Deafness, Femoral Epiphyseal Dysplasia, and Lacrimal Duct Obstruction GRW034
Growth Retardation, Developmental Delay, and Facial Dysmorphism GRW039 GDFD
Growth Retardation, Impaired Intellectual Development, Hypotonia, and Hepatopathy GRW040 GRIDHH
Growth Retardation, Small and Puffy Hands and Feet, and Eczema GRW033
Growth Retardation-Mild Developmental Delay-Chronic Hepatitis Syndrome GRW022
Grubben De Cock Borghgraef Syndrome GRB001
Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia GTP002
Guanylate Cyclase 2e, Pseudogene GNY003 GUCY2EP
Guanylate Kinase 3 GNY002 GUK3
Guillain-Barre Syndrome GLL022 GBS
Guillain-Barre Syndrome, Familial GLL037 GBS
Guizar Vasquez Sanchez Manzano Syndrome GZR001
Gum Cancer GMC001
Gummatous Syphilis GMM001
Gurrieri Syndrome GRR002
Guttate Psoriasis GTT002
Gynandroblastoma GYN003
Gynatresia GYN002
Gynecomastia GYN001
Gyrate Atrophy of Choroid and Retina GYR004 GACR
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