| 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 |
|
| Galactorrhea |
GLC096 |
|
| Galactorrhoea-Hyperprolactinaemia |
GLC025 |
|
| Galactosemia I |
GLC113 |
GALAC1 |
| Galactosemia Ii |
GLC111 |
GALAC2 |
| Galactosemia Iii |
GLC112 |
GALAC3 |
| Galactosemia Iv |
GLC115 |
GALAC4 |
| Galactosialidosis |
GLC012 |
GSL |
| Gallamine Allergy |
GLL044 |
|
| Gallbladder Adenocarcinoma |
GLL017 |
|
| Gallbladder Adenoma |
GLL029 |
|
| Gallbladder Angiosarcoma |
GLL002 |
|
| Gallbladder Benign Neoplasm |
GLL051 |
|
| Gallbladder Cancer |
GLL018 |
|
| Gallbladder Carcinoma in Situ |
GLL050 |
|
| 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 |
|
| 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 |
| Gand Syndrome |
GND017 |
GAND |
| 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 |
|
| Gatad2b-Associated Neurodevelopmental Disorder |
GTD002 |
|
| Gaucher Disease, Atypical, Due to Saposin C Deficiency |
GCH010 |
AGD |
| Gaucher Disease, Perinatal Lethal |
GCH018 |
GDPL |
| Gaucher Disease, Type I |
GCH015 |
GD1 |
| 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 |
| Gbe1 Adult Polyglucosan Body Disease |
GB1002 |
|
| Gcgr-Related Hyperglucagonemia |
GCG001 |
|
| Gdap1-Related Hereditary Motor and Sensory Neuropathy |
GDP003 |
|
| 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 Duplication Disease |
GND018 |
|
| 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 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 Hemolytic Uremic Syndrome |
GNT188 |
|
| Genetic Hyperaldosteronism |
GNT152 |
|
| Genetic Hyperferritinemia Without Iron Overload |
GNT037 |
|
| Genetic Hyperparathyroidism |
GNT127 |
|
| Genetic Hyperpigmentation of the Skin |
GNT091 |
|
| 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 |
|
| 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 Nephrotic Syndrome |
GNT182 |
|
| 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 Hypomagnesemia with Hypocalciuria |
GNT181 |
|
| Genetic Primary Hypomagnesemia with Normocalciuria |
GNT180 |
|
| Genetic Primary Orthostatic Disorder |
GNT171 |
|
| Genetic Primary Orthostatic Hypotension |
GNT144 |
|
| Genetic Prion Disease |
GNT189 |
|
| 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 Steroid-Resistant Nephrotic Syndrome |
GNT179 |
SRN1 |
| 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 a Major Feature |
GNT187 |
|
| Genetic Syndrome with a Cerebellar Malformation As a Major Feature |
GNT185 |
|
| Genetic Syndrome with a Dandy-Walker Malformation As a Major Feature |
GNT186 |
|
| 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 Systemic Disease with Glomerulopathy As a Major Feature |
GNT183 |
|
| 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 |
|
| Geniospasm 1 |
GNS004 |
GSM1 |
| Genital Dwarfism |
GNT015 |
|
| Genital Dwarfism, Turner Type |
GNT016 |
|
| Genital Herpes |
GNT003 |
|
| Genitopalatocardiac Syndrome |
GNT043 |
|
| Genitopatellar Syndrome |
GNT031 |
GTPTS |
| Genitourinary and/or Brain Malformation Syndrome |
GNT184 |
GUBS |
| 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 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 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 |
| Gjb1 Disorders: Charcot Marie Tooth Neuropathy and Central Nervous System Phenotypes |
GJB007 |
|
| Gjc2-Related Late-Onset Primary Lymphedema |
GJC002 |
|
| 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 Closed-Angle |
GLC114 |
GLCC |
| 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 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 |
|
| 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 |
| Glutamate-Cysteine Ligase Deficiency |
GLT040 |
|
| 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 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 1 |
GLY112 |
GPIBD1 |
| 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 |
| 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 |
|
| Gnao1-Related Developmental Delay-Seizures-Movement Disorder Spectrum |
GN1002 |
|
| Gnathodiaphyseal Dysplasia |
GNT026 |
GDD |
| Gnathomiasis |
GNT004 |
|
| Gnathostoma Infection |
GNT023 |
|
| Gnb1 Encephalopathy |
GNB001 |
|
| Gnptab-Related Disorders |
GNP002 |
|
| 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 |
| Gollop Coates Syndrome |
GLL023 |
|
| Gombo Syndrome |
GMB001 |
|
| Gomez-Lopez-Hernandez Syndrome |
GMZ002 |
GLHS |
| Gonadal Agenesis |
GND011 |
|
| 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 |
|
| Gout |
GT001 |
GOUT |
| Gracile Bone Dysplasia |
GRC002 |
GCLEB |
| Gracile Syndrome |
GRC001 |
GRACILE |
| Graft-Versus-Host Disease |
GRF003 |
GVHDS |
| Graham Boyle Troxell Syndrome |
GRH002 |
|
| Graham-Little-Piccardi-Lassueur Syndrome |
GRH005 |
|
| 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, Chronic, Autosomal Recessive, 1 |
GRN062 |
CGD1 |
| Granulomatous Disease, Chronic, Autosomal Recessive, 2 |
GRN063 |
CGD2 |
| Granulomatous Disease, Chronic, Autosomal Recessive, 3 |
GRN064 |
CGD3 |
| Granulomatous Disease, Chronic, Autosomal Recessive, 4 |
GRN061 |
CGD4 |
| Granulomatous Disease, Chronic, Autosomal Recessive, 5 |
GRN065 |
CGD5 |
| Granulomatous Disease, Chronic, X-Linked |
GRN051 |
CGDX |
| 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-Related Neurodevelopmental Disorder |
GRN056 |
|
| Grin2a-Related Speech Disorders and Epilepsy |
GRN041 |
|
| Grin2b-Related Developmental Delay, Intellectual Disability and Autism Spectrum Disorder |
GRN066 |
|
| 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 Frontotemporal Dementia |
GRN059 |
|
| Grn-Related Frontotemporal Lobar Degeneration |
GRN060 |
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 Syndrome with Immune Dysregulation 1 |
GRW043 |
|
| Growth Hormone Insensitivity Syndrome with Immune Dysregulation 1, Autosomal Recessive |
GRW041 |
GHISID1 |
| Growth Hormone Insensitivity Syndrome with Immune Dysregulation 2 |
GRW044 |
|
| Growth Hormone Insensitivity Syndrome with Immune Dysregulation 2, Autosomal Dominant |
GRW042 |
GHISID2 |
| Growth Hormone Insensitivity with Immunodeficiency |
GRW003 |
|
| Growth Hormone Insensitivity, Partial |
GRW026 |
GHIP |
| Growth Hormone Secreting Pituitary Adenoma |
GRW001 |
|
| 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 |
|
| 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 |
