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Disease	Synonyms	Description	Articles	Phenotypes
gnathodiaphyseal dysplasia	GDD; gnathodiaphyseal sclerosis; Levin syndrome 2; .. [+] gnathodiaphyseal sclerosis; GDD; Levin syndrome 2; osteogenesis imperfecta with unusual skeletal lesions; osteogenesis imperfecta, Levin type [-]	An osteochondrodysplasia characterized by cementoo..[+] An osteochondrodysplasia characterized by cementoosseous lesions of the jawbones, bone fragility, bowing/cortical thickening of tubular bones, and diaphyseal sclerosis of long bones that has_material_basis_in heterozygous mutation in the ANO5 gene on chromosome 11p14.3. [-]
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. [-]
Gillespie syndrome	GLSP; aniridia-cerebellar ataxia-intellectual disa.. [+] GLSP; aniridia-cerebellar ataxia-intellectual disability syndrome; aniridia, cerebellar ataxia and mental deficiency [-]	A syndrome characterized by iris hypoplasia, conge..[+] A syndrome characterized by iris hypoplasia, congenital hypotonia, cerebellar hypoplasia, variably cognitive impairment, and ataxia that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the ITPR1 gene on chromosome 3p26.1. [-]
Gordon Holmes syndrome	GDHS; CAHH; LHRH deficiency and ataxia; cerebellar.. [+] GDHS; CAHH; LHRH deficiency and ataxia; cerebellar ataxia-hypogonadism syndrome; luteinizing hormone-releasing hormone deficiency with ataxia [-]	An inherited metabolic disorder characterized by p..[+] An inherited metabolic disorder characterized by progressive cognitive decline, dementia, hypogonadotropic hypogonadism, and variable movement disorders resulting from disordered ubiquitination that has_material_basis_in homozygous or compound heterozygous mutation in the RNF216 gene on chromosome 7p22.1. [-]
Greenberg dysplasia	GRBGD; Greenberg skeletal dysplasia; autosomal rec.. [+] Greenberg skeletal dysplasia; GRBGD; autosomal recessive lethal chondrodystrophy with congenital hydrops; HEM dysplasia; hydrops-ectopic calcification-motheaten syndrome; Skeletal dysplasia, Greenberg type; hydrops, ectopic calcification, moth-eaten skeletal dysplasia [-]	An inherited metabolic disorder characterized by a..[+] An inherited metabolic disorder characterized by a defect in cholesterol biosynthesis resulting in fetal hydrops, severe shortening of all long bones with a moth-eaten radiographic appearance, platyspondyly, disorganization of chondroosseous calcification, and ectopic ossification centers that has_material_basis_in homozygous or compound heterozygous mutation in LBR on chromosome 1q42.12. [-]
glutamate formiminotransferase deficiency	Arakawa syndrome 1; FIGLUria; formiminoglutamic ac.. [+] Arakawa syndrome 1; FIGLUria; formiminoglutamic acidemia; formiminotransferase cyclodeaminase deficiency; FTCD deficiency; formiminotransferase deficiency syndrome; formiminoglutamic aciduria [-]	A vitamin metabolic disorder characterized by elev..[+] A vitamin metabolic disorder characterized by elevated formiminoglutamate in urine and plasma and variable intellectual, developmental, and hematological phenotypes that has_material_basis_in homozygous or compound heterozygous mutation in the FTCD gene on chromosome 21q22.3. [-]
glutamate-cysteine ligase deficiency	gamma-glutamylcysteine synthetase deficiency; hemo.. [+] gamma-glutamylcysteine synthetase deficiency; hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency [-]	An amino acid metabolic disorder characterized by ..[+] An amino acid metabolic disorder characterized by decreased levels of cellular glutathione and gamma-glutamylcysteine and hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the GCLC gene on chromosome 6p12.1. [-]
geleophysic dysplasia	geleophysic dwarfism; GPHYSD	A bone development disease characterized by short-..[+] A bone development disease characterized by short-limb dwarfism, brachydactyly, cardiac valvular disease, characteristic facial appearance, skin thickening, and laryngotracheal stenosis. [-]
geleophysic dysplasia 1	GPHYSD1	A geleophysic dysplasia that has_material_basis_in..[+] A geleophysic dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the ADAMTSL2 gene on chromosome 9q34.2. [-]
geleophysic dysplasia 2	GPHYSD2	A geleophysic dysplasia that has_material_basis_in..[+] A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1. [-]
geleophysic dysplasia 3	GPHYSD3	A geleophysic dysplasia that has_material_basis_in..[+] A geleophysic dysplasia that has_material_basis_in heterozygous mutation in the LTBP3 gene on chromosome 11q13.1. [-]
growth hormone secreting pituitary adenoma 2	GH-secreting pituitary adenoma 2; acromegaly due t.. [+] GH-secreting pituitary adenoma 2; acromegaly due to pituitary adenoma 2; PITA2; X-linked acromegaly [-]	A growth hormone secreting pituitary adenoma chara..[+] A growth hormone secreting pituitary adenoma characterized by adult-onset sporadic acromegaly and somatic somatotropinoma that has_material_basis_in mutation in the GPR101 gene on chromosome Xq26.3. [-]
glutaric acidemia type 3	glutaryl-CoA oxidase deficiency; glutaric aciduria.. [+] glutaryl-CoA oxidase deficiency; glutaric aciduria type 3; glutaric aciduria III; glutaric aciduria 3; GA3; GA III [-]	A peroxisomal disease characterized by isolated ac..[+] A peroxisomal disease characterized by isolated accumulation of glutaric acid in the absence of other clinical phenotype that has_material_basis_in homozygous or compound heterozygous mutation in the SUGCT gene on chromosome 7p14.1. [-]
GAPO syndrome	growth delay-alopecia-pseudoanodontia-optic atroph.. [+] growth delay-alopecia-pseudoanodontia-optic atrophy syndrome [-]	A syndrome characterized by growth retardation, al..[+] A syndrome characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations that has_material_basis_in homozygous or compound heterozygous mutation in the ANTXR1 gene on chromosome 2p13.3. [-]
Gaucher's disease type IIIC	Gaucher-like disease; GD3C; Gaucher disease-ophtha.. [+] GD3C; Gaucher-like disease; Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome; Gaucher disease type 3C; cardiovascular Gaucher disease [-]	A Gaucher's disease type III characterized by addi..[+] A Gaucher's disease type III characterized by additional presence of cardiovascular calcifications that has_material_basis_in homozygosity for an asp409-to-his (D409H) mutation in the GBA1 gene on chromosome 1q22. [-]
Ghosal hematodiaphyseal syndrome	Ghosal syndrome; Ghosal hematodiaphyseal dysplasia.. [+] Ghosal syndrome; Ghosal hematodiaphyseal dysplasia; diaphyseal dysplasia-anemia syndrome [-]	A syndrome characterized by increased bone density..[+] A syndrome characterized by increased bone density with predominant diaphyseal involvement and aregenerative corticosteroid-sensitive anemia that has_material_basis_in homozygous or compound heterozygous mutation in TBXAS1 on chromosome 7q34. [-]
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. [-]	24 articles
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. [-]	21 articles	44 matches
stomach disease	Gastropathy; gastric disease; stomach disorder	A gastrointestinal system disease that is located_..[+] A gastrointestinal system disease that is located_in the stomach. [-]	1 articles
benign giant cell tumor	Giant cell tumor NOS (morphologic abnormality); Gi.. [+] Giant cell tumor NOS (morphologic abnormality); Giant cell tumors (morphologic abnormality); Giant cell tumors; Giant cell tumor (qualifier value); Giant cell tumor (morphologic abnormality); Giant cell neoplasm; tumor of the Giant cell [-]	n_a
tenosynovial giant cell tumor	Giant cell tumour of tendon sheath; Giant cell tum.. [+] Giant cell tumour of tendon sheath; Giant cell tumor of tendon sheath; Giant cell tumour of Tenosynovium; Giant cell tumor of Tenosynovium; fibrous histiocytoma of tendon sheath (disorder); fibrous histiocytoma of tendon sheath; tenosynovial giant cell tumour [-]	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; Wide-angle .. [+] glaucoma simplex; open angle glaucoma; Wide-angle glaucoma; pigmentary 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	A primary open angle glaucoma early age of onset, ..[+] A primary open angle glaucoma early age of onset, rapidly progressive with more severely elevated and fluctuating intraocular pressures. [-]
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 one or more areas ..[+] A skin disease characterized by one or more areas of well-demarcated, non-pitting edema of deep subcutaneous tissues. [-]
status epilepticus	Grand mal status; (Grand mal status) or (status ep.. [+] Grand mal status; (Grand mal status) or (status epilepticus) [-]	n_a	1 articles
idiopathic generalized epilepsy	Generalised epilepsy	An epilepsy syndrome that is characterized by gene..[+] An epilepsy syndrome that is characterized by generalised seizures with no apparent cause which arise from many independent foci (multifocal epilepsies) or from epileptic circuits that involve the whole brain. [-]	10 articles
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	n_a
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; germ cell neoplasm of Ov.. [+] germ cell tumor of ovary; germ cell neoplasm of Ovary; germ cell tumor of ovary (disorder); 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; Thrombopathy, Bernard-Soulier; Hemorrhagic dystrophic thrombocytopenia [-]	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; Generalized multip.. [+] Generalized multiple sclerosis; 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. [-]	11 articles	4 matches
skin granular cell tumor	granular cell tumor of skin; granular cell tumour .. [+] granular cell tumor of skin; granular cell tumour of skin; granular cell tumor of skin (disorder); granular cell neoplasm of the skin; skin granular cell tumour [-]	n_a
cutaneous ganglioneuroma	Ganglioneuroma of skin; Ganglioneuroma of skin (di.. [+] Ganglioneuroma of skin; Ganglioneuroma of skin (disorder); Cutaneous Ganglioneuroma [-]	n_a
skin glomus tumor	Glomus tumor of skin; Glomus tumour of skin; Glomu.. [+] Glomus tumour of skin; Glomus tumor of skin; Glomus tumor of skin (disorder); Glomus skin neoplasm; skin glomus tumour [-]	n_a
skin glomangioma	Glomangioma of skin; Glomangioma of skin (disorder.. [+] Glomangioma of skin; 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; NBCCS; .. [+] Gorlin syndrome; basal cell nevus syndrome; NBCCS [-]	A syndrome characterized by multiple early-onset b..[+] A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities. [-]
malignant giant cell tumor of the tendon sheath	Giant cell tumour of tendon sheath, malignant; mal.. [+] Giant cell tumour of tendon sheath, malignant; malignant Giant cell neoplasm of the Tendon Sheath [-]	n_a
pseudoxanthoma elasticum	Gronblad-Strandberg syndrome	A connective tissue disease that is characterized ..[+] A connective tissue disease that is characterized by the accumulation of deposits of calcium and other minerals in elastic fibers, which are a component of connective tissue, this can result in changes in the skin, eyes, cardiovascular system and gastrointestinal system. [-]
stress polycythemia	Gaisbock's syndrome; Gaisbock's syndrome (disorder.. [+] Gaisbock's syndrome; Gaisbock's syndrome (disorder); Polycythemia, emotional; Stress polycythemia (disorder); Stress polycythemia [dup] (disorder); Stress polycythemia; Stress Polycythemia [-]	n_a
bruxism	Grinding teeth; sleep related bruxism; Teeth grind.. [+] Grinding teeth; sleep related bruxism; Teeth grinding; Bruxism - teeth grinding [-]	A sleep disorder that involves involuntarily grind..[+] A sleep disorder that involves involuntarily grinding or clenching of the teeth while sleeping. [-]
high grade glioma	glial cell tumor; glioma, malignant; Neuroglial tu.. [+] glioma, malignant; glial cell tumor; Neuroglial tumor; malignant Neuroglial tumor; malignant glioma [-]	A cell type cancer that has_material_basis_in glia..[+] A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. [-]	8 articles	8 matches
brain glioblastoma multiforme	Glioblastoma multiforme of brain; Glioblastoma mul.. [+] Glioblastoma multiforme of brain; Glioblastoma multiforme of brain (disorder); brain Glioblastoma [-]	A brain glioma that has_material_basis_in abnormal..[+] A brain glioma that has_material_basis_in abnormally proliferating cells derives_from glial cells, has_symptom seizure, headaches, nausea and vomiting, memory loss, changes to personality, mood or concentration; and localized neurological problems. [-]
anaplastic astrocytoma	grade III Astrocytic tumor; grade III astrocytoma; .. [+] grade III astrocytoma; grade III Astrocytic tumor; anaplastic astrocytoma [-]	A malignant astrocytoma that is characterized by c..[+] A malignant astrocytoma that is characterized by cells with regular, round to oval nuclei. [-]

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