congenital deficiency in alpha-fetoprotein

ORPHA: 168612

Overview

Congenital deficiency in alpha-fetoprotein is a benign genetic condition characterized by a dramatically decreased level of alpha-fetoprotein in fetus or neonate

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

Orphanet Code

ORPHA:168612
congenital deficiency in alpha-fetoprotein
OrphanetORPHA:168612
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
congenital deficiency in alpha-fetoprotein | OrphanDrug