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Diseases
Genes (1277)
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CFTR
Azoospermia
Vas Deferens, Congenital Bilateral Aplasia Of, X-Linked
Oligospermia
WRN
Werner Syndrome
Fanconi Anemia, Complementation Group D2
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
CFC1
Double Outlet Right Ventricle
Heterotaxy, Visceral, 8, Autosomal
ADGRG2
Azoospermia
Vas Deferens, Congenital Bilateral Aplasia Of, X-Linked
Oligospermia
ERCC4
Diplopia
Azoospermia
Werner Syndrome
Fanconi Anemia, Complementation Group D2
FANCM
Azoospermia
Fanconi Anemia, Complementation Group D2
BRIP1
Azoospermia
Werner Syndrome
Fanconi Anemia, Complementation Group D2
FANCD2
Azoospermia
Werner Syndrome
Fanconi Anemia, Complementation Group D2
SLX4
Azoospermia
Fanconi Anemia, Complementation Group D2
FANCL
Azoospermia
Fanconi Anemia, Complementation Group D2
FANCG
Azoospermia
Fanconi Anemia, Complementation Group D2
FANCC
Azoospermia
Fanconi Anemia, Complementation Group D2
FANCA
Azoospermia
Fanconi Anemia, Complementation Group D2
GDF1
Double Outlet Right Ventricle
Heterotaxy, Visceral, 8, Autosomal
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
RAD51
Azoospermia
Werner Syndrome
Fanconi Anemia, Complementation Group D2
BRCA1
Azoospermia
Werner Syndrome
Fanconi Anemia, Complementation Group D2
Oligospermia
RAD51C
Azoospermia
Fanconi Anemia, Complementation Group D2