Xenbase

Search Diseases

Alphabetic Search:

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 ???pagination.result.next???

Disease	Synonyms	Description	Articles	Phenotypes
benign familial infantile seizures 5	Benign Familial Infantile Seizures, 5;	A benign familial infantile epilepsy that is chara..[+] A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the SCN8A gene on chromosome 12q13. [-]
benign familial infantile seizures 6	Autosomal dominant nocturnal frontal lobe epilepsy.. [+] Autosomal dominant nocturnal frontal lobe epilepsy; Benign Familial Infantile Seizures, 6; nocturnal frontal lobe epilepsy-4; [-]	A benign familial infantile epilepsy that is chara..[+] A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the CHRNA2 gene on chromosome 8p21. [-]
benign familial neonatal epilepsy	familial neonatal seizures (disorder); familial ne.. [+] familial neonatal seizures (disorder); familial neonatal seizures; [-]	n_a	3 articles
benign fibrous mesothelioma	fibrous mesothelioma, benign (morphologic abnormal.. [+] fibrous mesothelioma, benign (morphologic abnormality); fibrous mesothelioma, benign; localized benign fibrous Mesothelioma; [-]	n_a
benign giant cell tumor	Giant cell neoplasm; Giant cell tumor (morphologic.. [+] Giant cell neoplasm; Giant cell tumor (morphologic abnormality); Giant cell tumor (qualifier value); Giant cell tumors; Giant cell tumors (morphologic abnormality); tumor of the Giant cell; Giant cell tumor NOS (morphologic abnormality); [-]	n_a
benign hypertensive renal disease	benign hypertensive renal disease (disorder); hype.. [+] benign hypertensive renal disease (disorder); hypertensive renal disease, benign, without mention of renal failure; hypertensive renal disease, benign; [-]	n_a
benign ileal neoplasm	Ileal tumor;	A small intestine benign neoplasm that affects the..[+] A small intestine benign neoplasm that affects the wall of the ileum. [-]
benign intermediate mesothelioma	Well-differentiated Papillary tumor of Mesothelium.. [+] Well-differentiated Papillary tumor of Mesothelium; [-]	n_a
benign lymphoepithelial lesion of salivary gland	benign lymphoepithelial lesion of salivary gland (.. [+] benign lymphoepithelial lesion of salivary gland (disorder); Godwin tumor; [-]	n_a
benign mammary dysplasia		n_a
benign mastocytoma	benign Mastocytoma;	n_a
benign meningioma	meningioma, benign;	n_a
benign mesothelioma	benign tumor of Mesothelium;	A cell type benign neoplasm that has_material_basi..[+] A cell type benign neoplasm that has_material_basis_in mesothelium. [-]
benign neonatal seizures	benign neonatal convulsions; benign familial neona.. [+] benign neonatal convulsions; benign familial neonatal seizures; [-]	A neonatal period electroclinical syndrome that is..[+] A neonatal period electroclinical syndrome that is characterized by tonic-clonic seizures in newborns occurring within the first seven days of life and ceasing within the first 15 weeks of life and has_material_basis_in autosomal dominant inheritance of voltage-gated potassium channels or a chromosomal inversion. [-]	2 articles
benign neoplasm		A disease of cellular proliferation that results i..[+] A disease of cellular proliferation that results in abnormal growths in the body which lack the ability to metastasize. [-]	7 articles	4 matches
benign paroxysmal positional vertigo	benign paroxysmal positional vertigo; benign parox.. [+] benign paroxysmal positional vertigo; benign paroxysmal positional nystagmus; benign recurrent vertigo; [-]	A peripheral vertigo that is characterized by epis..[+] A peripheral vertigo that is characterized by episodic vertigo followed by gait imbalance and oscillopsia with profound bilateral vestibular loss despite normal hearing. [-]
benign pericardial teratoma	Mature teratoma of Pericardium;	n_a
benign peritoneal mesothelioma	Mesothelioma of Peritoneum;	n_a
benign peritoneal solitary fibrous tumor		A peritoneal benign neoplasm that is characterized..[+] A peritoneal benign neoplasm that is characterized by the presence of prominent hemangiopericytoma-like vessels. [-]
benign perivascular tumor		n_a
benign pleural mesothelioma	Mesothelioma of Pleura;	n_a
benign prostate phyllodes tumor	Phyllodes neoplasm of the prostate; prostate phyll.. [+] Phyllodes neoplasm of the prostate; prostate phyllodes tumor; benign Phyllodes neoplasm of the prostate; prostate phyllodes tumour; benign prostate phyllodes tumour; [-]	n_a
benign recurrent intrahepatic cholestasis	BRIC; Summerskill-Walshe-Tygstrup syndrome;	An intrahepatic cholestasis characterized by inter..[+] An intrahepatic cholestasis characterized by intermittent, recurrent episodes of intrahepatic cholestasis mostly without progression to liver damage or extrahepatic bile duct obstruction. [-]
benign recurrent intrahepatic cholestasis 1	BRIC type 1; BRIC1; Summerskill syndrome;	A benign recurrent intrahepatic cholestasis charac..[+] A benign recurrent intrahepatic cholestasis characterized by typically autosomal recessive inheritance that has_material_basis_in mutation in the ATP8B1 gene on chromosome 18q. [-]
benign recurrent intrahepatic cholestasis 2	BRIC type 2; BRIC2;	A benign recurrent intrahepatic cholestasis charac..[+] A benign recurrent intrahepatic cholestasis characterized by autosomal recessive inheritance that has_material_basis_in mutation in the ABCB11 gene on chromosome 2q31. [-]
benign renovascular hypertension		n_a
benign secondary hypertension		n_a
benign shuddering attacks		n_a
benign teratoma		A germ cell benign neoplasm that derives_from matu..[+] A germ cell benign neoplasm that derives_from mature tissue elements or a limited amount of immature tissue elements. [-]
benign vaginal carcinosarcoma		A vaginal benign neoplasm that has_material_basis_..[+] A vaginal benign neoplasm that has_material_basis_in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components. [-]
benzoic acid allergic contact dermatitis	allergic contact dermatitis to benzoate;	An allergic contact dermatitis that has_allergic_t..[+] An allergic contact dermatitis that has_allergic_trigger benzoic acid. [-]
benzylpenicillin allergy	benzyl benicillin allergy; penicillin G allergy; b.. [+] benzyl benicillin allergy; penicillin G allergy; benzyl penicillin allergy; [-]	A beta-lactam allergy that has_allergic_trigger be..[+] A beta-lactam allergy that has_allergic_trigger benzylpenicillin. [-]
beriberi		A thiamine deficiency disease that is characterize..[+] A thiamine deficiency disease that is characterized by being severe and chronic. [-]
berylliosis	beryllium poisoning;	A pneumoconiosis that involves allergic response l..[+] A pneumoconiosis that involves allergic response located_in lungs caused by inhalation of beryllium compounds. [-]
bestiality	Zoophilia;	n_a
bestrophinopathy	autosomal recessive bestrophinopathy;	n_a
beta thalassemia		A thalassemia characterized by the reduced or abse..[+] A thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin. [-]	1 articles
beta-ketothiolase deficiency	2-methyl-3-hydroxybutyricacidemia; Mitochondrial a.. [+] 2-methyl-3-hydroxybutyricacidemia; Mitochondrial acetoacetyl-CoA Thiolase deficiency; 3-ketothiolase deficiency; 3-oxothiolase deficiency; alpha-methylacetoaceticaciduria; peroxisomal thiolase deficiency (disorder); peroxisomal thiolase deficiency; [-]	An amino acid metabolic disorder characterized by ..[+] An amino acid metabolic disorder characterized by inability to process isoleucine and ketones, has_symptom recurrent ketoacidotic attacks in infancy marked by vomitting, lethargy, dehydration, and seizures, and has_material_basis_in mutation in the ACAT1 gene of chromosome 11q22.3 responsible for producing the ACAT1 enzyme in mitochondria, which processes isoleucine and ketones. [-]
beta-lactam allergy		A drug allergy triggered by a beta-lactam.
beta-mannosidosis	lysosomal beta-mannosidase deficiency; Beta-D-mann.. [+] lysosomal beta-mannosidase deficiency; Beta-D-mannosidosis (disorder); Beta-D-mannosidosis; beta-mannosidase deficiency; [-]	A lysosomal storage disease that has_material_basi..[+] A lysosomal storage disease that has_material_basis_in deficiency of the beta-A-manosidase enzyme resulting in the disruption of N-linked glycoprotein oligosaccharide catabolism. [-]
beta-thalassemia intermedia		A beta thalassemia that is characterized by mild t..[+] A beta thalassemia that is characterized by mild to moderate anemia along with slow growth and bone abnormalities appearing in early childhood or later in life. [-]
beta-thalassemia major	Cooley's anemia;	A beta thalassemia that is characterized by severe..[+] A beta thalassemia that is characterized by severe anemia and enlarged liver and spleen before 2 years of age. [-]
bicipital tenosynovitis		n_a
bicuspid aortic valve disease	Familial bicuspid aortic valve;	An aortic valve disease that is characterized by t..[+] An aortic valve disease that is characterized by the presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives. [-]
bilateral breast cancer	Bilateral breast carcinoma;	A breast carcinoma that is characterized by an ind..[+] A breast carcinoma that is characterized by an individual having breast cancer in both breasts, either simultaneously or at different times. [-]
bilateral frontal polymicrogyria		A polymicrogyria that is characterized as a symmet..[+] A polymicrogyria that is characterized as a symmetric and bilateral form (in both brain hemispheres) that only involves the frontal lobes without including the area located behind the Sylvius fissure or the area located behind the Rolando sulcus. Symptoms included delayed motor and language milestones; spastic (stiffness) hemiparesis (weakness in one side of the body) or quadriparesis (weakness in all four limbs of the body); and mild to moderate intellectual disability. [-]
bilateral frontoparietal polymicrogyria		A polymicrogyria that is characterized by excessiv..[+] A polymicrogyria that is characterized by excessive cortical folding and abnormal cortical layering, that involves the frontoparietal region of the brain and that presents with hypotonia, developmental delay, moderate to severe intellectual disability, pyramidal signs, epileptic seizures, non progressive cerebellar ataxia, dysconjugate gaze and/or strabismus and that has_material_basis_in homozygous mutation in the ADGRG1 gene on chromosome 16q21. [-]
bilateral hyperactive labyrinth	Bilateral hyperactive labyrinth (disorder); hypera.. [+] Bilateral hyperactive labyrinth (disorder); hyperactive bilateral labyrinthine dysfunction (disorder); hyperactive bilateral labyrinthine dysfunction; hyperactive labyrinth, bilateral; Bilateral hyperactive labyrinth; [-]	n_a
bilateral hypoactive labyrinth	Hypoactive bilateral labyrinthine dysfunction (dis.. [+] Hypoactive bilateral labyrinthine dysfunction (disorder); Hypoactive labyrinth, bilateral; Bilateral hypoactive labyrinth (disorder); Bilateral hypoactive labyrinth; Hypoactive bilateral labyrinthine dysfunction; [-]	n_a
bilateral meningioma of optic nerve	Bilateral meningioma of the optic nerve;	n_a

???pagination.result.page??? ???pagination.result.prev??? 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 ???pagination.result.next???