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Disease	Synonyms	Description
glutathione synthetase deficiency		An amino acid metabolic disorder characterized by ..[+] An amino acid metabolic disorder characterized by the lack of glutathione production. [-]
gene duplication disease	gene duplication syndrome	A monogenic disease that is the result of a mutati..[+] A monogenic disease that is the result of a mutation that involves the production of one or more copies of a gene. [-]
glycogen-rich carcinoma		A breast adenocarcinoma characterized by the prese..[+] A breast adenocarcinoma characterized by the presence of malignant epithelial cells with abundant clear cytoplasm which contains glycogen. [-]
glutatione synthetase deficiency with 5-oxoprolinuria		A glutathione synthetase deficiency that is charac..[+] A glutathione synthetase deficiency that is characterized by massive urinary excretion of 5-oxoproline, metabolic acidosis, hemolytic anemia, and central nervous system damage and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding glutathione synthetase (GSS) on chromosome 20q11. The metabolic defect results in decreased levels of cellular glutathione, which overstimulates the synthesis of gamma-glutamylcysteine and its subsequent conversion to 5-oxoproline. [-]
Graves ophthalmopathy	Graves orbitopathy; Thyroid associated ophthalmopa.. [+] Graves orbitopathy; Thyroid associated ophthalmopathy; thyroid eye disease [-]	An autoimmune disease of eyes, ear, nose and throa..[+] An autoimmune disease of eyes, ear, nose and throat that is characterized by upper eyelid retraction, lid lag, swelling, redness, conjunctivitis, and bulging eyes. [-]
grade I lymphomatoid granulomatosis		A lymphomatoid granulomatosis that is characterize..[+] A lymphomatoid granulomatosis that is characterized by the presence of a polymorphous lymphoid infiltrate without cytologic atypia. Large lymphocytes are absent or rare. By in situ hybridization, EBV-positive cells are infrequently seen. [-]
grade III lymphomatoid granulomatosis		A lymphomatoid granulomatosis that is characterize..[+] A lymphomatoid granulomatosis that is characterized by the presence of aggregates of neoplastic large B-lymphocytes, usually admixed with pleomorphic and Hodgkin-like cells, in a background of chronic inflammation. Necrotic changes are present and are usually extensive. [-]
glycogen storage disease Ib		A glycogen storage disease I that has_material_bas..[+] A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PT1 gene (SLC37A4), which encodes glucose-6-phosphate translocase, on chromosome 11q23. [-]
giant axonal neuropathy 1		An axonal neuopathy characterized by autosomal rec..[+] An axonal neuopathy characterized by autosomal recessive inheritance of progressive motor and sensitive peripheral, central nervous system neuropathy.with axonal loss and giant axonal swellings filled with neurofilaments that has_material_basis_in homozygous or compound heterozygous mutation in the GAN gene on chromosome 16q23 [-]
giant axonal neuropathy 2		An axonal neuopathy characterized by autosomal dom..[+] An axonal neuopathy characterized by autosomal dominant inheritance of distal sensory impairment, lower extremity muscle weakness and atrophy, and giant axonal swelling with neurofilament accumulation that has_material_basis_in heterozygous mutation in the DCAF8 gene on chromosome 1q23 [-]
Gaucher's disease type I	GD I; Glucocerebrosidase Deficiency; GD1; Gba Defi.. [+] GD1; Glucocerebrosidase Deficiency; GD I; Gba Deficiency; Gaucher Disease, Noncerebral Juvenile; Acid Beta-Glucosidase Deficiency [-]	A Gaucher's disease characterized by absence of pr..[+] A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22. [-]
Gaucher's disease type II	Gaucher Disease, Acute Neuronopathic Type; GD II; .. [+] GD II; Gaucher Disease, Acute Neuronopathic Type; Infantile Cerebral Gaucher Disease [-]	A Gaucher's disease characterized by rapid neurolo..[+] A Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has_material_basis_in an autosomal recessive mutation of GBA on chromosome 1q22. [-]
Gaucher's disease type III	GD III; Gaucher Disease, Subacute Neuronopathic Ty.. [+] GD III; Gaucher Disease, Subacute Neuronopathic Type; Gaucher Disease, Juvenile And Adult, Cerebral; Gaucher Disease, Chronic Neuronopathic Type [-]	A Gaucher's disease characterized by later onset a..[+] A Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22. [-]
Gaucher's disease perinatal lethal	Gaucher Disease, Collodion Type; Fetal Gaucher Dis.. [+] Gaucher Disease, Collodion Type; Fetal Gaucher Disease [-]	A Gaucher's Disease characterized by perinatal let..[+] A Gaucher's Disease characterized by perinatal lethality and rapid progression of neurological deterioration that has_material_basis_in an autosomal recessive mutation of GBA on chromosome 1q22. [-]
glycine N-methyltransferase deficiency	GNMT deficiency; hypermethioninemia due to glycine.. [+] GNMT deficiency; hypermethioninemia due to glycine N-methyltransferase deficiency; hypermethioninemia due to GNMT deficiency [-]	A hypermethioninemia characterized by autosomal re..[+] A hypermethioninemia characterized by autosomal recessive inheritance of persistent isolated hypermethioninemia without cystathionine beta-synthase deficiency, tyrosinemia type I, or liver disease that has_material_basis_in homozygous or compound heterozygous mutation in the GNMT gene on chromosome 6p21. [-]
glycogen storage disease IXd	GSD type 9E; GSD type IXd; GSD type IXe; GSD9D; GS.. [+] GSD9D; GSD type IXe; GSD type IXd; GSD type 9E; GSD type 9D; GSD IXd; GSD due to muscle phosphorylase kinase deficiency; glycogenosis type IXe; glycogenosis type IXd; glycogenosis type 9E; glycogenosis type 9D; glycogenosis due to muscle phosphorylase kinase deficiency; glycogen storage disease type IXe; glycogen storage disease type IXd; glycogen storage disease type 9E; glycogen storage disease type 9D; glycogen storage disease due to muscle phosphorylase kinase deficiency; muscle phosphorylase kinase deficiency; X-linked muscke glycogenosis [-]	A glycogen storage disease IX characterized by X-l..[+] A glycogen storage disease IX characterized by X-linked inheritance of variable exercise-induced muscle weakness or stiffness that has material_basis_in mutation in the PHKA1 gene on chromosome Xq13. [-]
glycogen storage disease IXb	GSD IXb; GSD type 9B; GSD type IXb; GSD9B; GSD due.. [+] GSD9B; GSD type IXb; GSD type 9B; GSD IXb; GSD due to liver and muscle phosphorylase kinase deficiency; glycogenosis type IXb; glycogenosis type 9B; glycogenosis due to liver and muscle phosphorylase kinase deficiency; glycogen storage disease type IXb; glycogen storage disease type 9B [-]	A glycogen storage disease IX characterized by aut..[+] A glycogen storage disease IX characterized by autosomal recessive inheritance of hepatomegaly, short stature, hypotonia and accumulation of glycogen in both liver and muscle, without clinical symptoms, that has material_basis_in compound heterozygous mutation in the PHKB gene on chromosome 16q12. [-]
glycogen storage disease IXa	GSD type 9A; GSD type IXa; GSD9A; glycogenosis typ.. [+] GSD9A; GSD type IXa; GSD type 9A; glycogenosis type IXa; glycogenosis type 9A; glycogen storage disease type IXa; glycogen storage disease type 9A [-]	A glycogen storage disease IX characterized by X-l..[+] A glycogen storage disease IX characterized by X-linked inheritance of hepatomegaly, growth retardation, elevation of glutamate-pyruvate transaminase and glutamate-oxaloacetate transaminase, hypercholesterolemia, hypertriglyceridemia, and fasting hyperketosis, but symptoms gradually disappear with age, that has material_basis_in mutation in the PHKA2 gene on chromosome Xp22. [-]
glycogen storage disease IXc	GSD type 9C; GSD type IXc; GSD9C; glycogenosis typ.. [+] GSD9C; GSD type IXc; GSD type 9C; glycogenosis type IXc; glycogenosis type 9C; glycogen storage disease type IXc; glycogen storage disease type 9C [-]	A glycogen storage disease IX characterized by aut..[+] A glycogen storage disease IX characterized by autosomal recessive inheritance of hepatomegaly, hypotonia, growth retardation, and liver dysfunction with onset in childhood and improvement of symptoms with age that has material_basis_in homozygous and compound heterozygous mutation in the PHKG2 gene on chromosome 16p11. [-]
gray platelet syndrome	GPS; BDPLT4; platelet alpha-granule deficiency; pl.. [+] GPS; BDPLT4; platelet alpha-granule deficiency; platelet-type bleeding disorder 4 [-]	An inherited blood coagulation disease characteriz..[+] An inherited blood coagulation disease characterized by selective deficiency in the number and contents of platelet alpha-granules, macrothrombocytopenia, enlarged platelets, myelofibrosis, splenomegaly, and increased bleeding time that has material_basis_in homozygous or compound heterozygous mutation in the NBEAL2 gene on chromosome 3p21. [-]
globozoospermia	male infertility due to globozoospermia; male infe.. [+] male infertility due to globozoospermia; male infertility due to round-headed spermatozoa [-]	A male infertility characterized by round-headed s..[+] A male infertility characterized by round-headed spermatozoa lacking an acrosome. [-]
generalized epilepsy with febrile seizures plus 10	generalized epilepsy with febrile seizures plus ty.. [+] generalized epilepsy with febrile seizures plus type 10; generalised epilepsy with febrile seizures plus type 10; generalised epilepsy with febrile seizures plus 10; GEFSP10; GEFS+10 [-]	A generalized epilepsy with febrile seizures plus ..[+] A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in HCN1 on chromosome 5p12. [-]
generalized epilepsy with febrile seizures plus 8	generalized epilepsy with febrile seizures plus ty.. [+] generalized epilepsy with febrile seizures plus type 8; generalised epilepsy with febrile seizures plus type 8; generalised epilepsy with febrile seizures plus 8; GEFSP8; GEFS+8 [-]	A generalized epilepsy with febrile seizures plus ..[+] A generalized epilepsy with febrile seizures plus that has_material_basis_in variation in a region on chromosome 6q16.3-q22.31. [-]
generalized epilepsy with febrile seizures plus 1	generalized epilepsy with febrile seizures plus ty.. [+] generalized epilepsy with febrile seizures plus type 1; generalised epilepsy with febrile seizures plus type 1; generalised epilepsy with febrile seizures plus 1; GEFSP1; GEFS+1 [-]	A generalized epilepsy with febrile seizures plus ..[+] A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN1B on chromosome 19q13.11. [-]
Guttmacher syndrome	autosomal dominant preaxial deficiency, postaxial .. [+] autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias; preaxial deficiency-postaxial polydactyly-hypospadias syndrome [-]	A syndrome characterized by preaxial deficiencies ..[+] A syndrome characterized by preaxial deficiencies of the hands and feet, postaxial polydactyly of the hands, and hypospadias that has_material_basis_in heterozygous mutation in the HOXA13 gene on chromosome 7p15.2. [-]
glutathione synthetase deficiency of erythrocytes	glutathione synthetase deficiency without 5-oxopro.. [+] glutathione synthetase deficiency without 5-oxoprolinuria [-]	A glutathione synthetase deficiency characterized ..[+] A glutathione synthetase deficiency characterized by hemolytic anemia and deficiency in GSH that is limited to the red blood cells, with nucleated cells able to maintain normal or near normal expression levels that has_material_basis_in homozygous or compound heterozygous mutation in GSS on chromosome 20q11.22. [-]
reproductive system disease	genital system disease	A disease of anatomical entity that is located_in ..[+] A disease of anatomical entity that is located_in reproductive system organs. [-]
skin disease	Genodermatosis; skin and subcutaneous tissue disea.. [+] Genodermatosis; skin and subcutaneous tissue disease [-]	An integumentary system disease that is located_in..[+] An integumentary system disease that is located_in skin. [-]
stomach disease	Gastropathy; gastric disease; stomach disorder	A gastrointestinal system disease that is located_..[+] A gastrointestinal system disease that is located_in the stomach. [-]
tenosynovial giant cell tumor	Giant cell tumor of Tenosynovium; Giant cell tumor.. [+] Giant cell tumor of Tenosynovium; Giant cell tumor of tendon sheath; fibrous histiocytoma of tendon sheath (disorder) [-]	n_a
active peptic ulcer disease	GI Bleeding	n_a
bacterial pneumonia	gram-negative pneumonia; Pneumonia due to other gr.. [+] gram-negative pneumonia; Pneumonia due to other gram-negative bacteria [-]	A pneumonia involving inflammation of the lungs ca..[+] A pneumonia involving inflammation of the lungs caused by bacteria. [-]
open-angle glaucoma	glaucoma simplex; open angle glaucoma; pigmentary .. [+] glaucoma simplex; open angle glaucoma; pigmentary glaucoma; Wide-angle glaucoma [-]	A glaucoma characterized by optic nerve damage res..[+] A glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage. [-]
juvenile glaucoma	Glaucoma of childhood	n_a
atrophic glossitis	Glossitis, Hunter's; Atrophy of tongue papillae; H.. [+] Glossitis, Hunter's; Atrophy of tongue papillae; Hunter's glossitis; smooth atrophic tongue [-]	n_a
chronic gonorrhea of cervix	Gonococcal cervicitis, chronic; chronic gonococcal.. [+] Gonococcal cervicitis, chronic; chronic gonococcal cervicitis [-]	A chronic cervicitis that is caused by gonorrhea.
angioedema	giant urticaria; angioneurotic edema; Angioneuroti.. [+] giant urticaria; angioneurotic edema; Angioneurotic oedema; Quincke's edema [-]	A skin disease characterized by the rapid swelling..[+] A skin disease characterized by the rapid swelling of the dermis, subcutaneous tissue, mucosa and submucosal tissues. [-]
idiopathic generalized epilepsy	Generalised epilepsy	An epilepsy syndrome that is characterised by gene..[+] An epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from many independent foci (multifocal epilepsies) or from epileptic circuits that involve the whole brain. [-]
focal dermal hypoplasia	Goltz-Gorlin syndrome; Goltz syndrome; FDH; FODH	A syndrome characterized at birth by streaks of ve..[+] A syndrome characterized at birth by streaks of very thin skin (dermal hypoplasia), cutis aplasia, and telangiectases, and has_material_basis_in heterozygous mutation in the PORCN gene on chromosome Xp11.23. [-]
brain germinoma	germinoma of the brain; intracranial germinoma	A brain cancer that is characterized by abnormally..[+] A brain cancer that is characterized by abnormally proliferating cells, derives_from germ cells. [-]
urogenital tuberculosis	Genitourinary tuberculosis	An extrapulmonary tuberculosis that is located_in ..[+] An extrapulmonary tuberculosis that is located_in urogenital system. [-]
ovarian germ cell cancer	germ cell tumor of ovary (disorder); germ cell neo.. [+] germ cell tumor of ovary (disorder); germ cell neoplasm of Ovary; ovarian germ cell tumor [-]	An ovarian cancer that originates in the germ (egg..[+] An ovarian cancer that originates in the germ (egg) cells of the ovary. [-]
Bernard-Soulier syndrome	Giant platelet syndrome; Giant platelet syndrome (.. [+] Giant platelet syndrome; Giant platelet syndrome (disorder); Bernard - Soulier thrombopathy; Bernard Soulier syndrome; Hemorrhagic dystrophic thrombocytopenia; Thrombopathy, Bernard-Soulier [-]	A blood coagulation disease characterized by autos..[+] A blood coagulation disease characterized by autosomal recessive inheritance of mucosal bleeding, purpuric skin bleeding, epistaxis, and menorrhagia with prolonged bleeding times, enlarged platelets and absence of platelet aggregation in response to von Willebrand factor that has_material_basis_in mutation in the GP1BA gene, the GP1BB gene, or the GP9 gene which are subunits of the platelet membrane von Willebrand factor receptor complex, glycoprotein Ib. [-]
multiple sclerosis	Generalized multiple sclerosis (disorder); insular.. [+] Generalized multiple sclerosis (disorder); insular sclerosis [-]	A demyelinating disease that involves damage to th..[+] A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. [-]
skin granular cell tumor	granular cell tumor of skin (disorder); granular c.. [+] granular cell tumor of skin (disorder); granular cell neoplasm of the skin [-]	n_a
cutaneous ganglioneuroma	Ganglioneuroma of skin (disorder); Cutaneous Gangl.. [+] Ganglioneuroma of skin (disorder); Cutaneous Ganglioneuroma [-]	n_a
skin glomus tumor	Glomus tumor of skin (disorder); Glomus skin neopl.. [+] Glomus tumor of skin (disorder); Glomus skin neoplasm [-]	n_a
skin glomangioma	Glomangioma of skin (disorder); Cutaneous Glomangi.. [+] Glomangioma of skin (disorder); Cutaneous Glomangioma [-]	n_a
tooth erosion	generalized erosion; localized erosion	n_a
nevoid basal cell carcinoma syndrome	Gorlin syndrome; basal cell nevus syndrome	n_a

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