CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C1835362 | Lp(A) Deficiency, Congenital | MSH | Lp(A) Deficiency, Congenital | C563618 |
C1835362 | Lp(A) Deficiency, Congenital | OMIM | Lp(a) DEFICIENCY, CONGENITAL | 152200 |
CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C1835362 | Lp(A) Deficiency, Congenital | MSH | Lp(A) Deficiency, Congenital | C563618 |
C1835362 | Lp(A) Deficiency, Congenital | OMIM | Lp(a) DEFICIENCY, CONGENITAL | 152200 |