Fanconi anemia complementation group A

MONDO:0009215

Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides instructions for making a protein that is involved in the Fanconi anemia (FA) pathway.

Also known as: FANCA, FANCA Fanconi anaemia, FANCA Fanconi anemia, Fanconi Anemia, complementation group type a, Fanconi anaemia caused by mutation in FANCA, Fanconi anaemia complementation group type A, Fanconi anemia caused by mutation in FANCA, Fanconi anemia complementation group A

16 clinical trials for this condition and its sub-types, 4 tagged with Fanconi anemia complementation group A itself.

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Where it sits in the disease tree

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Part of

↑ Fanconi anemia (42) ↑ Non-syndromic limb reduction defect (35)

Including sub-types (16) Tagged with Fanconi anemia complementation group A (4)

Not yet recruiting 1 Not yet finished but already full! 2 Terminated 1

A simple brush could spot mouth cancer early in fanconi anaemia patients

Diagnosis Not yet recruiting

People with Fanconi anaemia have a high risk of developing oral cancer, but standard biopsies are painful and risky due to their genetic sensitivity. This study tests a non-invasive oral brushing technique to detect early cancer cells in 115 patients aged 15 and older. If accurat…

Sponsor: Institut Jean-Godinot • Aim: Diagnosis

Last updated Jun 27, 2026 07:58 UTC

Fanconi anemia complementation group A

Where it sits in the disease tree

A simple brush could spot mouth cancer early in fanconi anaemia patients