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| Paediatric disorders - additional genes v0.35 | CRELD1 | Ellen McDonagh reviewed gene: CRELD1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Atrioventricular septal defect, partial, with heterotaxy syndrome, Atrioventricular septal defect, susceptibility to, 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Paediatric disorders - additional genes v0.34 | CRELD1 |
Ellen McDonagh gene: CRELD1 was added gene: CRELD1 was added to Paediatric disorders - additional genes. Sources: South West GLH Mode of inheritance for gene: CRELD1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: CRELD1 were set to Atrioventricular septal defect, partial, with heterotaxy syndrome; Atrioventricular septal defect, susceptibility to, 2 |
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