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Congenital deficiency in alpha-fetoprotein
Disease definition
Congenital deficiency in alpha-fetoprotein is a benign genetic condition characterized by a dramatically decreased level of alpha-fetoprotein in fetus or neonate.
ORPHA:168612
Classification level: Disorder- Synonym(s): -
- Prevalence: <1 / 1 000 000
- Inheritance: -
- Age of onset: Antenatal, Neonatal
- ICD-10: -
- OMIM: 615969
- UMLS: C1863081
- MeSH: -
- GARD: -
- MedDRA: -
Additional information
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