| Disease Browser
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Parent Node:
 Anemia, Hemolytic (D000743) |
Parent Node:
Genetic Diseases, Inborn (D030342) |
..Starting node
.. Anemia, Hemolytic, Congenital (D000745)
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Child Nodes:
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........Anemia, Dyserythropoietic, Congenital (D000742)  5 |
| ........Anemia, Hemolytic, Congenital Nonspherocytic (D000746) 5 |
| ........Anemia, hereditary spherocytic hemolytic (C536356) |
| ........Anemia, Sickle Cell (D000755) 3 |
| ........Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema (C566369) |
| ........Elliptocytosis, Hereditary (D004612) 11 |
| ........Glucosephosphate Dehydrogenase Deficiency (D005955) 3 |
| ........Heinz Body Anemias (C563030) |
| ........Hemoglobin C Disease (D006445) 1 |
| ........Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa (C562629) |
| ........Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities (C563935) |
| ........HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY (OMIM:613470) |
| ........Red cell phospholipid defect with hemolysis (C535298) |
| ........Rh-Null Disease, Amorph Type (C566210) |
| ........Spherocytosis, Hereditary (D013103) 5 |
| ........Stomatocytosis I (C566111) |
| ........Stomatocytosis II (C566110) |
| ........Thalassemia (D013789) 16 |
| ........Transient erythroblastopenia of childhood (C536980) |
| ........Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to (C564859) |
| ........Xerocytosis, hereditary (C536764) |
Sister Nodes: |
..ACTH Deficiency, Isolated (C562707)
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..Adrenal Hyperplasia, Congenital (D000312) 12
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..Adrenocortical Hypofunction, Chronic Primary Congenital (C562711)
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..Alagille Syndrome (D016738)
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..alpha 1-Antitrypsin Deficiency (D019896) 1
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..Alpha-2-Deficient Collagen Disease (C565963)
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..Anemia, Hemolytic, Congenital (D000745) 68
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..Anemia, Hypoplastic, Congenital (D029502) 27
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..Angioedemas, Hereditary (D054179) 2
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..Ataxia Telangiectasia (D001260) 6
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..Atrial Standstill (C563984)
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..Autoimmune Lymphoproliferative Syndrome (D056735) 5
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..Blood Coagulation Disorders, Inherited (D025861) 70
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..Brugada Syndrome (D053840) 9
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..CADASIL (D046589) 1
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..Camurati-Engelmann Syndrome (D003966) 4
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..Cardiomyopathy, Hypertrophic, Familial (D024741) 15
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..Cerebral Palsy, Ataxic, Autosomal Recessive (C562856)
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..CHARGE Syndrome (D058747)
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..Cherubism (D002636) 2
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..Chromosome Disorders (D025063) 160
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..Cirrhosis, Familial (C566123)
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..Complement Factor I Deficiency (C572568)
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..Corticosteroid-Binding Globulin Deficiency (C565152)
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..Costello Syndrome (D056685)
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..Cryoglobulinemia, Familial Mixed (C565141)
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..Cystic Fibrosis (D003550) 4
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..Donohue Syndrome (D056731) 1
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..Dwarfism (D004392) 155
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..Epistaxis, Hereditary (C562751)
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..Eye Diseases, Hereditary (D015785) 373
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..Frasier Syndrome (D052159)
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..Genetic Diseases, X-Linked (D040181) 412
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..Genetic Diseases, Y-Linked (D050174) 5
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..Hajdu-Cheney Syndrome (D031845) 1
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..Hemoglobinopathies (D006453) 23
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..Hepatic Fibrosis, Congenital (C562378)
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..Hereditary Autoinflammatory Diseases (D056660) 10
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..Hereditary Myopathy with Early Respiratory Failure (C566343)
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..Heredodegenerative Disorders, Nervous System (D020271) 543
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..Histiocytosis, Familial Lipochrome (C562738)
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..Hyper-IgM Immunodeficiency Syndrome (D053306) 3
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..Hyperthyroxinemia, Familial Dysalbuminemic (D050010) 1
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..Interstitial Pneumonitis, Desquamative, Familial (C562470)
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..Kallmann Syndrome (D017436) 9
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..Kartagener Syndrome (D007619) 6
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..Lennox Gastaut Syndrome (D065768) 1
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..Loeys-Dietz Syndrome (D055947) 5
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..Marfan Syndrome (D008382) 9
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..Metabolism, Inborn Errors (D008661) 886
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..Muscular Dystrophies (D009136) 117
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..Myasthenic Syndromes, Congenital (D020294) 15
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..Nail-Patella Syndrome (D009261) 1
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..Neoplastic Syndromes, Hereditary (D009386) 111
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..Neutropenia, Nonimmune Chronic Idiopathic, Adult (C564320)
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..Osteoarthropathy, Primary Hypertrophic (D010004) 2
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..Osteogenesis Imperfecta (D010013) 27
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..Pain Insensitivity, Congenital (D000699) 2
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..Parotidomegaly, Hereditary Bilateral (C566821)
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..Pelger-Huet Anomaly (D010381)
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..Platelet Glycoprotein IV Deficiency (C564245)
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..Polycystic Kidney, Autosomal Recessive (D017044) 3
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..Prolactin Deficiency, Isolated (C562708)
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..Pulmonary Alveolar Microlithiasis (C562405)
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..Pycnodysostosis (D058631)
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..Rh Deficiency Syndrome (C562717)
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..Skin Diseases, Genetic (D012873) 462
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..Weill-Marchesani Syndrome (D056846)
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..Werner Syndrome (D014898) 1
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..Yellow Nail Syndrome (D056684) 1
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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