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table started by tfmorris for the tfmorris's Base
A temporary flagging type for topics which are likely duplicates and should be reviewed for merger
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x Vitamin E Deficiency (leading to 1-Methylhistidinuria)    
x Adrenal Cortical Dysfunction (11B-hydroxylase Deficiency)    
x 11-Hydroxylase Deficiency    
x 17-Hydroxylase Deficiency    
x Vitamin B6 (Riboflavin) Deficiency    
x Intestinal Resection    
x Carcinoid Tumors    
x 3-Hydroxyisobutyric Aciduria    
x Beta-Ureidopropionase (UP) Deficiency    
x Combined Uraciluria-Thyminuria    
x Phenylketonuria III    
x Biotin Deficiency Results in Mental Changes (Depression, Hallucinations), Paresthesia, Anorexia, and Nausea    
x 3-Beta-Hydroxysteroid Dehydrogenase Deficiency    
x 21-hydroxylase Deficiency (cyp21): increased    
x Corticosterone Methyl Oxidase I Deficiency (CMO I)    
x Corticosterone Methyl Oxidase II Deficiency (CMO II)    
x Corticosterone Methyl Oxidase II Deficiency - CMO II: decreased    
x Deficiency of Various Neurotransmitters in the Central Nervous System    
x Hyperphenylalaninemia    
x Thalassemia Trait    
x Tumour Necrosis    
x Antidiuresis    
x Pediatric traumatic brain injury    
x Uroporphyria    
x Paediatric short-bowel syndrome    
x Neurally Mediated Syncope    
x 3-Hydroxy-3-Methylglutaric Acidemia    
x 3-Methyl-Crotonyl-Glycinuria    
x 3-Methylglutaconic Aciduria (Type IV)    
x Acrodermatitis Enterohepathica    
x Adenosylcobalamin Deficiency (CBLA, CBLB)    
x Anticonvulasant Hypersensitivity Syndrome Valproate Associated Hepatotoxicity (in valproate therapy)    
x Carnitine Deficiency, Myopathic    
x Citrullinemia Type II, Adult-Onset    
x Delta-Pyrrolidine-5-Carboxylate Synthase Deficiency    
x Hyperinsulinism-Hyperammonemia Syndrome    
x Liver Disease, Liver Failure, Unspecific    
x Patent Ductus Venosus    
x Pyruvate Dehydrogenase Deficiency (E2)    
x Pyruvate Dehydrogenase Deficiency (E3)    
x Reye Syndrome Like Manifestations    
x Argininosuccinic Acid Lyase Deficiency    
x Argininosuccinyl-CoA lyase deficiency    
x Citrullinemia Type II    
x Hydroxylase Deficiency    
x Coprostanic Acidemia    
x Crigler-Najjar Syndrome, Types I and II    
x Intoxication Acetaminophen [DD]    
x Trihydroxycoprostanic Acidemia    
x Hypoxic-ischemic encephalopathy    
x Idiopathic polyneuritis    
x Serous meningitis    
x Ketosis, Unspecific [DD]    
x Feeding: Veganian [DD]    
x Lethal Infantile Cardiomyopathy: X-Linked Cardioskeletal Myopathy (Barth Syndrome)    
x Long Chain Acyl-Coa Dehydrogenase Deficiency (LCAD)    
x Valproate Therapy: Anticonvulasant Hypersensitivity Syndrome Valproate Associated Hepatotoxicity    
x 17-alpha-hydroxylase Deficiency (cyp17)    
x Isolated ACTH Deficiency    
x Addison Disease, X-Linked    
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