Disease Browser
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Parent Node: Heart Septal Defects, Atrial (D006344) |
..Starting node ..Atrial Septal Defect Sinus Venosus (C548009)
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Child Nodes:
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Sister Nodes: |
..3C syndrome (C535313)
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..Atrial Septal Defect 1 (C566239)
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..Atrial septal defect 2 (C538263)
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..Atrial Septal Defect 3 (C563540)
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..Atrial Septal Defect 4 (C566963)
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..Atrial Septal Defect 5 (C567561)
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..Atrial Septal Defect 6 (C567764)
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..Atrial Septal Defect Ostium Primum (C548006)
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..Atrial Septal Defect Sinus Venosus (C548009)
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..Atrial Septal Defect with Atrioventricular Conduction Defects (C566238) 1
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..Atrial Septal Defect, Primum Type (C566240)
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..Atrial Septal Defect, Secundum Type (C566241)
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..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
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..Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss (C537789)
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..Ciuffo Syndrome (C566733)
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..Dursun Syndrome (C567804)
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..Foramen Ovale, Patent (D054092)
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..Holt-Oram syndrome (C535326)
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..Irons Bhan syndrome (C535539)
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..Lutembacher Syndrome (D008185)
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..Lymphedema, Cardiac Septal Defects, And Characteristic Facies (C567398)
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..Oculootofacial Dysplasia (C563682)
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..Radial Ray Deficiency, X-Linked (C564523)
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..Rapadilino syndrome (C535288)
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..Tel Hashomer camptodactyly syndrome (C536953)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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