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Atrial septal defect, ostium primum type
2 OMIM references -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Atrial septal defect, ostium secundum type
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
- ASD, ostium primum type
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
2 OMIM references -
1 MeSH reference: C548006
Gene symbol UniProt reference OMIM reference
TLL1 O43897606742
No signs/symptoms info available.