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MIM:606217 - ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2; AVSD2
Xenbase Genes: creld1
Human Disease Resource: MIM
| MONDO:0011650 - atrioventricular septal defect, susceptibility to, 2 |
| MONDO:0020290 - familial atrioventricular septal defect |
