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.

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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