Disease #04302 (FANCS (Fanconi anemia, complementation group S (FANCS)))

Official abbreviation FANCS
Name Fanconi anemia, complementation group S (FANCS)
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Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene BRCA1
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Individuals

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00074676 - PubMed: Sawyer 2015 - F no Finland - - 0 - - FANCS hypertelorism, epicanthal folds, ptosis, strabismus, blepharophimosis, broad nasal bridge and nasal tip, and proximally inserted thumbs - BRCA1 2 1 Arleen D. Auerbach
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