ASD8
MCID: ATR065
MIFTS: 24
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Atrial Septal Defect 8 (ASD8)
Categories:
Cardiovascular diseases, Genetic diseases
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MalaCards integrated aliases for Atrial Septal Defect 8:
Characteristics:HPO:31Classifications:
ICD10:
32
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UniProtKB/Swiss-Prot :
73
Atrial septal defect 8: A congenital heart malformation characterized by incomplete closure of the wall between the atria resulting in blood flow from the left to the right atria.
MalaCards based summary : Atrial Septal Defect 8, is also known as asd8. An important gene associated with Atrial Septal Defect 8 is CITED2 (Cbp/P300 Interacting Transactivator With Glu/Asp Rich Carboxy-Terminal Domain 2). Affiliated tissues include heart, and related phenotypes are atrial septal defect and anomalous pulmonary venous return Disease Ontology : 12 An atrial heart septal defect that has material basis in heterozygous mutation in the CITED2 gene on chromosome 6q23.3. |
Diseases in the Atrial Septal Defect 2 family:
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Human phenotypes related to Atrial Septal Defect 8:31 (showing 2, show less)
Symptoms via clinical synopsis from OMIM:56Clinical features from OMIM:614433GenomeRNAi Phenotypes related to Atrial Septal Defect 8 according to GeneCards Suite gene sharing:26 (showing 8, show less)
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Interventional clinical trials:(showing 1, show less)
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MalaCards organs/tissues related to Atrial Septal Defect 8:40
Heart
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Articles related to Atrial Septal Defect 8:(showing 9, show less)
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ClinVar genetic disease variations for Atrial Septal Defect 8:6 (showing 3, show less)
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Search
GEO
for disease gene expression data for Atrial Septal Defect 8.
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