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Complete atrioventricular canal - left heart obstruction
2 associated genes
31 connected diseases
No signs/symptoms info
Disease Type of connection
Complete atrioventricular canal - Fallot tetralogy
Complete atrioventricular canal - ventricle hypoplasia
Partial atrioventricular canal
Tetralogy of Fallot
Atrial septal defect, ostium secundum type
Familial atrial fibrillation
Single ventricular septal defect
46,XY partial gonadal dysgenesis
8p23.1 microdeletion syndrome
Athyreosis
Atrial septal defect - atrioventricular conduction defects
Familial isolated congenital asplenia
Familial progressive cardiac conduction defect
Hypoplastic left heart syndrome
Thyroid hypoplasia
Congenital diaphragmatic hernia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
46,XX gonadal dysgenesis
46,XY complete gonadal dysgenesis
Holt-Oram syndrome
Distal 22q11.2 microdeletion syndrome
17q11 microdeletion syndrome
Familial exudative vitreoretinopathy
Frontonasal dysplasia with alopecia and genital anomaly
Isolated scaphocephaly
Kabuki syndrome
Parietal foramina
Potocki-Shaffer syndrome
Weaver syndrome
5q14.3 microdeletion syndrome
Berardinelli-Seip congenital lipodystrophy
Synonym(s):
- CAVC - left heart obstruction
- CAVC type A
- Complete atrioventricular canal type A
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
CRELD1 Q96HD1607170
GATA4 P43694600576
No signs/symptoms info available.