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Items: 2

1.

Alpha-fetoprotein deficiency

Alpha-fetoprotein deficiency appears to be a benign genetic trait (Greenberg et al., 1992; Sharony et al., 2004). [from OMIM]

MedGen UID:
354899
Concept ID:
C1863081
Disease or Syndrome
2.

Alpha-fetoprotein, hereditary persistence of

Hereditary persistence of alpha-fetoprotein (HPAFP) is a clinically benign autosomal dominant condition characterized by continued expression of alpha-fetoprotein in adult life (summary by McVey et al., 1993). [from OMIM]

MedGen UID:
349670
Concept ID:
C1863080
Finding

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