Details of Disease | DrugMAP

General Information of Disease (ID: DISB8IN0)

Disease Name	Obsolete congenital deficiency in alpha-fetoprotein
Synonyms	ALPHA-fetoprotein deficiency; AFPD
Definition	OBSOLETE. Congenital deficiency in alpha-fetoprotein is a benign genetic condition characterized by a dramatically decreased level of alpha-fetoprotein in fetus or neonate.\|This is a biological anomaly and not a disease.
Disease Hierarchy	DIS01GPL: Grass pollen hypersensitivity DISB8IN0: Obsolete congenital deficiency in alpha-fetoprotein

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
AFP	TTCFEA1	No Known	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
AFP	OT9GG3ZI	No Known	Autosomal recessive	[1]
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References

1	Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.