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Diseases
Genes (1491)
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ADAR
Dyschromatosis Symmetrica Hereditaria
Skin Condition
MAGEL2
Prader–willi Syndrome
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
CFAP43
Spermatogenic Failure 19
SNRPN
Prader–willi Syndrome
KRT17
Pachyonychia Congenita
SS18
Synovial Sarcoma
KRT16
Pachyonychia Congenita
Skin Condition
G6PD
Hemolytic Anemia
NDN
Prader–willi Syndrome
BCL2
Synovial Sarcoma
Primary Ovarian Insufficiency
TPI1
Hemolytic Anemia
FMR1
Primary Ovarian Insufficiency
Prader–willi Syndrome
SLC4A1
Hemolytic Anemia
KRT6A
Pachyonychia Congenita
GCLC
Hemolytic Anemia
AVP
Polyuria
Prader–willi Syndrome
BMP15
Primary Ovarian Insufficiency
NR5A1
Primary Ovarian Insufficiency