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Disease	Synonyms	Description	Articles	Phenotypes
Greig cephalopolysyndactyly syndrome	polysyndactyly with peculiars skull shape	An acrocephalosyndactylia that has_material_basis_..[+] An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face. [-]	2 articles
gallamine allergy		A drug allergy that has_allergic_trigger gallamine..[+] A drug allergy that has_allergic_trigger gallamine. [-]
granulomatous amebic encephalitis	granulomatous amoebic encephalitis; Granulomatous .. [+] granulomatous amoebic encephalitis; Granulomatous Amebic Encephalitis due to Acanthamoeba; Acanthamoeba encephalitis; Acanthamoeba granulomatous encephalitis [-]	A parasitic protozoa infectious disease that resul..[+] A parasitic protozoa infectious disease that results in infection of the brain caused by Acanthamoeba or Balamuthia mandrillaris. The symptoms include headaches, altered mental status, and focal neurologic deficit, which progresses over several weeks to death. [-]
glandular tularemia		A tularemia that results_in swelling of regional l..[+] A tularemia that results_in swelling of regional lymph glands. [-]
Gitelman syndrome	HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, W.. [+] HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA [-]	A renal tubular transport disease that is has_mate..[+] A renal tubular transport disease that is has_material_basis_in mutations in genes that produce proteins involved in the kidneys' reabsorption of salt (sodium chloride or NaCl) from urine back into the bloodstream, thus impairing the kidneys' ability to reabsorb salt, leading to the loss of excess salt in the urine (salt wasting). [-]	5 articles
Gamstorp-Wohlfart syndrome	autosomal recessive neuromyotonia and axonal neuro.. [+] autosomal recessive neuromyotonia and axonal neuropathy; myokymia, myotonia and muscle wasting [-]	A syndrome characterized by progressive weakness a..[+] A syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs. [-]	1 articles
glycogen storage disease XV	Glycogen storage disease with severe cardiomyopath.. [+] Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency; Glycogen storage disease 15; glycogen storage disease type XV [-]	A glycogen storage disease characterized by muscle..[+] A glycogen storage disease characterized by muscle weakness and cardiac abnormalities caused and has_material_basis_in mutation in the GYG1 gene that encodes glycogenin-1. [-]
gummatous syphilis		A tertiary syphilis that is characterized by granu..[+] A tertiary syphilis that is characterized by granulomatous lesions, called gummas, which are characterized by a center of necrotic tissue with a rubbery texture. They form in the liver, bones, and testes but may affect any organ. [-]
glycogen storage disease IX	Glycogen storage disease 9	A glycogen storage disease characterized by defici..[+] A glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity. [-]
gallbladder carcinoma in situ		An in situ carcinoma located_in the surface epithe..[+] An in situ carcinoma located_in the surface epithelium of the gallbladder that most commonly develops into adenocarcinoma. [-]
gastrointestinal system benign neoplasm		An organ system benign neoplasm located_in gastroi..[+] An organ system benign neoplasm located_in gastrointestinal tract organs. [-]
gastrointestinal neuroendocrine tumor	gastrointestinal neuroendocrine tumour; malignant .. [+] gastrointestinal neuroendocrine tumour; malignant gastrointestinal neuroendocrine tumor; malignant gastrointestinal neuroendocrine tumour [-]	A gastrointestinal system cancer that has_material..[+] A gastrointestinal system cancer that has_material_basis_in neuroendocrine cells. [-]
glycogen metabolism disorder		A carbohydrate metabolism disorder that is charact..[+] A carbohydrate metabolism disorder that is characterized by abnormal accumulation or depletion of liver glycogen. [-]
guanidinoacetate methyltransferase deficiency	GAMT deficiency; CEREBRAL CREATINE DEFICIENCY SYND.. [+] GAMT deficiency; CEREBRAL CREATINE DEFICIENCY SYNDROME 2; Cerebral creatine deficiency syndrome 2 [-]	A cerebral creatine deficiency syndrome that is ch..[+] A cerebral creatine deficiency syndrome that is characterized by severe intellectual disability, seizures, speech problems and involuntary movements, has_material_basis_in homozygous or compound heterozygous mutation in the GAMT gene on chromosome 19p13. [-]
glioblastoma classical subtype		A glioblastoma multiforme that is characterized by..[+] A glioblastoma multiforme that is characterized by abnormally high levels of epidermal growth factor receptor and the absence of p53 mutations. [-]
glioblastoma proneural subtype		A glioblastoma that is characterized by IDH1 and p..[+] A glioblastoma that is characterized by IDH1 and p53 mutations and Platelet Derived Growth Factor A amplification. [-]
glioblastoma mesenchymal subtype		A glioblastoma multiforme that is characterized by..[+] A glioblastoma multiforme that is characterized by the most frequent number of mutation of the Neurofibromin 1 gene. [-]
glioblastoma neural subtype		A glioblastoma that is characterized by the expres..[+] A glioblastoma that is characterized by the expression of several gene types that are also typical of the brain's normal, noncancerous nerve cells, or neurons. [-]
generalized dystonia	Dystonia 12; dystonia musculorum deformans; famili.. [+] Dystonia 12; dystonia musculorum deformans; familial dystonia; fragments of torsion dystonia; idiopathic familial dystonia; Idiopathic torsion dystonia; symptomatic torsion dystonia; dystonia deformans progressiva; idiopathic non-familial dystonia [-]	A dystonia that affects most or all of the body.
glomerulosclerosis		A glomerulonephritis that is characterized by hard..[+] A glomerulonephritis that is characterized by hardening of the glomerulus in the kidney. [-]
gallbladder adenoma		A gallbladder benign neoplasm that has_material_ba..[+] A gallbladder benign neoplasm that has_material_basis_in epithelial tissue of glandular origin located_in the gallbladder. [-]
gastrointestinal carcinoma		A gastrointestinal system cancer that has_material..[+] A gastrointestinal system cancer that has_material_basis_in epithelial cells. [-]
GRID2-related spinocerebellar ataxia		n_a
Good syndrome	thymoma with hypogammaglobulinemia	A combined T cell and B cell immunodeficiency that..[+] A combined T cell and B cell immunodeficiency that is a condition where there is co-occurrence of deficient cell-mediated immunity and benign thymoma. [-]
gluten allergy	gluten allergic reaction; allergy to gluten	A food allergy that develops from an immune reacti..[+] A food allergy that develops from an immune reaction to eating gluten, a protein found in wheat, barley, rye and triticale and that is characterized by stomach cramping, diarrhea and gastrointestinal upset and is unrelated to the gluten intolerance. [-]
gamma heavy chain disease	Franklin's disease	A heavy chain disease that results from an overpro..[+] A heavy chain disease that results from an overproduction of gamma antibody (IgG). [-]
generalized epilepsy with febrile seizures plus	GEFS+	An idiopathic generalized epilepsy that is charact..[+] An idiopathic generalized epilepsy that is characterized by febrile seizures often with accessory afebrile generalized tonic-clonic seizures with childhood onset. [-]	3 articles
GABA aminotransferase deficiency	gamma-aminobutyric acid transaminase deficiency; G.. [+] gamma-aminobutyric acid transaminase deficiency; Gamma-amino butyric acid transaminase deficiency [-]	A gamma-amino butyric acid metabolism disorder tha..[+] A gamma-amino butyric acid metabolism disorder that is characterized by a defect in the gene coding for gamma-aminobutyrate transaminase, which is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde. [-]
gamma-amino butyric acid metabolism disorder		An amino acid metabolic disorder characterized by ..[+] An amino acid metabolic disorder characterized by impairment of the GABA catabolic pathway. [-]
gastroduodenal Crohn's disease	upper GI Crohn's disease	An inflammatory bowel disease characterized by inf..[+] An inflammatory bowel disease characterized by inflammation located_in stomach and located_in duodenum, has_symptom nausea, has_symptom vomiting, has_symptom weight loss and has_symptom loss of appetite. [-]
gallbladder disease		A gastrointestinal system disease that is located_..[+] A gastrointestinal system disease that is located_in the gallbladder. [-]
glucocorticoid-induced osteoporosis	steroid-induced osteoporosis	An osteoporosis caused by chronic glucocorticoid u..[+] An osteoporosis caused by chronic glucocorticoid use. Glucocorticoids impair the replication, differentiation and function of osteoblasts and induce the apoptosis of mature osteoblasts and osteocytes; the also favor osteoclastogenesis leading to an increase in bone resorption. [-]
glycerol kinase deficiency		An inherited metabolic disorder characterized_by w..[+] An inherited metabolic disorder characterized_by wide range of phenotypic variability; patients can have severe metabolic and CNS abnormalities, while others possess hyperglycerolemia and glyceroluria with no other apparent phenotype and that has_material_basis_in mutation in the GK gene on chromosome Xp21. [-]
Galloway-Mowat syndrome 1	Galloway syndrome; nephrosis-microcephaly syndrome.. [+] Galloway syndrome; nephrosis-microcephaly syndrome; nephrosis-neuronal dysmigration syndrome; microcephaly, hiatal hernia and nephrotic syndrome; autosomal recessive spinocerebellar ataxia 5; SCAR5 [-]	A Galloway-Mowat syndrome that has_material_basis_..[+] A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25. [-]	2 articles	21 matches
granular corneal dystrophy 2	granular corneal dystrophy type 2; CGD2; avellino .. [+] granular corneal dystrophy type 2; CGD2; avellino corneal dystrophy; corneal dystrophy, Avellino type; combined granular-lattice corneal dystrophy [-]	An corneal granular dystrophy that is characterize..[+] An corneal granular dystrophy that is characterized by recurrent erosions and stellate or thorn-like opacification located_in the cornea, hyaline and amyloid deposits in the stroma, and progressive vision loss later in life, and has_material_basis_in autosomal dominant inheritance of mutation of transforming growth factor beta-induced gene on chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased hyaline and amyloid protein deposition and disruption of the corneal surface. [-]
gelatinous drop-like corneal dystrophy	GDCD; primary familial amyloidosis of the cornea; .. [+] GDCD; primary familial amyloidosis of the cornea; subepithelial amyloidosis of the cornea; corneal amyloidosis [-]	An epithelial and subepithelial dystrophy that is ..[+] An epithelial and subepithelial dystrophy that is characterized by severe corneal amyloidosis leading to blindness and that has_material_basis_in homozygous or compound heterozygous mutation in the TACSTD2 gene which encodes the monoclonal antibody-defined, tumor-associated antigen GA733-1, on chromosome 1p32. [-]
gingival fibromatosis	hereditary gingival fibromatosis; hereditary gingi.. [+] hereditary gingival fibromatosis; hereditary gingival hyperplasia [-]	A gingival overgrowth characterized by benign, slo..[+] A gingival overgrowth characterized by benign, slowly progressive, nonhemorrhagic, fibrous enlargement of the oral masticatory mucosa. [-]
Goldberg-Shprintzen syndrome	Goldberg-Shprintzen megacolon syndrome	A syndrome characterized by intellectual disabilit..[+] A syndrome characterized by intellectual disability, specific facial gestalt and Hirschsprung's disease and that has_material_basis_in homozygous mutation in the KIAA1279 gene on chromosome 10q21.1. [-]
gastrointestinal allergy		A hypersensitivity reaction type I disease located..[+] A hypersensitivity reaction type I disease located in the gastrointestinal tract. [-]
goat milk allergy	Capra hircus milk allergy	A milk allergy triggered by Capra hircus milk.
green mud crab allergy	Scylla paramamosain allergy	A crustacean allergy triggered by Scylla paramamos..[+] A crustacean allergy triggered by Scylla paramamosain. [-]
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		A frontotemporal dementia characterized by variabl..[+] A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31. [-]
Griscelli syndrome	Griscelli-Prunieras syndrome; Griscelli-PruniÃ©ras.. [+] Griscelli-Prunieras syndrome; Griscelli-PruniÃ©ras syndrome; ChÃ©diak-Higashi-like syndrome; Chediak-Higashi-like syndrome; partial albinism-immunodeficiency syndrome [-]	An integumentary system disease characterized by s..[+] An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin. [-]
Griscelli syndrome type 1	Griscelli-Prunieras syndrome type 1; Griscelli syn.. [+] Griscelli-Prunieras syndrome type 1; Griscelli syndrome with neurological impairment; GS1; Griscelli-PruniÃ©ras syndrome type 1; Griscelli syndrome, cutaneous and neurological type; hypopigmentation-neurologic impairment syndrome [-]	A Griscelli syndrome characterized by silvery gray..[+] A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and neurological impairment without immunodeficiency that has_material_basis_in mutations in the MYO5A gene on chromosome 15q21.2. [-]
Griscelli syndrome type 2	GS2; Griscelli-Prunieras syndrome type 2; Griscell.. [+] Griscelli-Prunieras syndrome type 2; GS2; Griscelli-PruniÃ©ras syndrome type 2; Griscelli syndrome with hemophagocytic syndrome; PAID syndrome; partial albinism and immunodeficiency syndrome; hypopigmentation-immunodeficiency with or without neurologic impairment syndrome [-]	A Griscelli syndrome characterized by silvery gray..[+] A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has_material_basis_in mutation in the RAB27A gene on chromosome 15q21.3. [-]
Griscelli syndrome type 3	GS3; Griscelli-Prunieras syndrome type 3; Griscell.. [+] Griscelli-Prunieras syndrome type 3; GS3; Griscelli-PruniÃ©ras syndrome type 3 [-]	A Griscelli syndrome characterized by isolated sil..[+] A Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has_material_basis_in mutation in the MLPH or MYO5A genes. [-]
GAND syndrome	autosomal dominant mental retardation 18; MRD18; a.. [+] autosomal dominant mental retardation 18; MRD18; autosomal dominant intellectual developmental disorder 18; autosomal dominant non-syndromic intellectual disability 18 [-]	An autosomal dominant intellectual developmental d..[+] An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy, with motor delay and moderate to severely impaired intellectual development and that has_material_basis_in an autosomal dominant mutation of the GATAD2B gene on chromosome 1q21.3. [-]
Galloway-Mowat syndrome 2		A Galloway-Mowat syndrome that has_material_basis_..[+] A Galloway-Mowat syndrome that has_material_basis_in hemizygous mutation in the LAGE3 gene on chromosome Xq28. [-]
Galloway-Mowat syndrome 3		A Galloway-Mowat syndrome that has_material_basis_..[+] A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11. [-]
Galloway-Mowat syndrome 4		A Galloway-Mowat syndrome that has_material_basis_..[+] A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13. [-]

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