| 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
|
