| Disease Browser
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Parent Node:
 Heart Septal Defects, Atrial (D006344) | ..Starting node
.. Lutembacher Syndrome (D008185)
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Child Nodes:
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Sister Nodes: | ..3C syndrome (C535313)
| ..Atrial Septal Defect 1 (C566239)
| ..Atrial septal defect 2 (C538263)
| ..Atrial Septal Defect 3 (C563540)
| ..Atrial Septal Defect 4 (C566963)
| ..Atrial Septal Defect 5 (C567561)
| ..Atrial Septal Defect 6 (C567764)
| ..Atrial Septal Defect Ostium Primum (C548006)
| ..Atrial Septal Defect Sinus Venosus (C548009)
| ..Atrial Septal Defect with Atrioventricular Conduction Defects (C566238)  1
| ..Atrial Septal Defect, Primum Type (C566240)
| ..Atrial Septal Defect, Secundum Type (C566241)
| ..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
| ..Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss (C537789)
| ..Ciuffo Syndrome (C566733)
| ..Dursun Syndrome (C567804)
| ..Foramen Ovale, Patent (D054092)
| ..Holt-Oram syndrome (C535326)
| ..Irons Bhan syndrome (C535539)
| ..Lutembacher Syndrome (D008185)
| ..Lymphedema, Cardiac Septal Defects, And Characteristic Facies (C567398)
| ..Oculootofacial Dysplasia (C563682)
| ..Radial Ray Deficiency, X-Linked (C564523)
| ..Rapadilino syndrome (C535288)
| ..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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| Term ID: | 6575 |
| Name: | Lutembacher Syndrome |
| Definition: | A condition characterized by a combination of OSTIUM SECUNDUM ATRIAL SEPTAL DEFECT and an acquired MITRAL VALVE STENOSIS. |
| Alternative IDs: | |
| ParentIDs: | MESH:D006344 |
| TreeNumbers: | C14.240.400.560.375.518 |C14.280.400.560.375.518 |C16.131.240.400.560.375.518 |
| Synonyms: | Lutembacher's Syndrome |Lutembachers Syndrome |Syndrome, Lutembacher |Syndrome, Lutembacher's |
| Slim Mappings: | Cardiovascular disease|Congenital abnormality |
| Reference: |
MedGen: D008185
MeSH: D008185
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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