" /> Fanconi anemia, complementation group V - CISMeF





Preferred Label : Fanconi anemia, complementation group V;

Symbol : FANCV;

CISMeF acronym : FANCV;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the mitotic arrest-deficient 2 like 2 gene (MAD2L2, 604094.0001);

Laboratory abnormalities : Chromosome instability; Increased serum alpha-fetoprotein; Increased chromosomal breakage in response to DNA crosslinking agents;

Prefixed ID : #617243;

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10/05/2025


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