Alpha-fetoprotein Deficiency; Afpd
Description
Congenital deficiency in alpha-fetoprotein is a benign genetic condition characterized by a dramatically decreased level of alpha-fetoprotein in fetus or neonate.
Genes related to Alpha-fetoprotein Deficiency; Afpd
- AFP
Clinical Features
Phenotypes and symptoms related to Alpha-fetoprotein Deficiency; Afpd
- Decreased levels of alpha-fetoprotein
Incidence and onset information
— Not enough data available about incidence and published cases.

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Alpha-fetoprotein Deficiency; Afpd Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Intellectual Disability NGS Panel.
By Fulgent Genetics Fulgent Genetics in United States.
BRCA2, F5, FMR1, MTHFR, TTR, UBE3A, PTEN, MCCC1, MCCC2, AGL, ACAT1, GYS2, ARG1, ATP7A, AUH, BCS1L, ADSL, FBLN5, LRP5, COL1A2 , (...)
View the complete list with 372 more genes
Specificity
1 %
Genes
100 % |
AFP.
By Fulgent Genetics Fulgent Genetics in United States.
AFP
Specificity
100 %
Genes
100 % |
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