Fh: congenital cvs anomaly (& [heart disease])
SCTID: 137815001, Primitive, Inactive
137815001 |Fh: congenital cvs anomaly (& [heart disease])|
516207018 - FH: Congenital CVS anomaly (& [heart disease]) (en) View
2712455013 - FH: Congenital CVS anomaly (& [heart disease]) (situation) (en) View
219010013 - FH: Congenital CVS anomaly (en) View
219009015 - FH: Congenital CVS anomaly (& [heart disease]) (en) View
219011012 - FH: Congenital heart disease (en) View
219012017 - FH: heart dis. congen. (en) View
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