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Diseases
Genes (1029)
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SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
ADAR
Dyschromatosis Symmetrica Hereditaria
CTNNB1
Pilomatricoma
MAPT
Supranuclear Palsy, Progressive, 1
KRT17
Pachyonychia Congenita
KRT16
Pachyonychia Congenita
CRYAA
Cataract 41
ACE
Severe Acute Respiratory Syndrome
Primary Ovarian Insufficiency
Dyschromatosis Symmetrica Hereditaria
Supranuclear Palsy, Progressive, 1
FMR1
Primary Ovarian Insufficiency
Supranuclear Palsy, Progressive, 1
STX6
Supranuclear Palsy, Progressive, 1
BMP15
Primary Ovarian Insufficiency
NR5A1
Primary Ovarian Insufficiency
POF1B
Primary Ovarian Insufficiency
NOBOX
Primary Ovarian Insufficiency
GDF9
Primary Ovarian Insufficiency
MOBP
Supranuclear Palsy, Progressive, 1
GJA8
Cataract 41
EIF2AK3
Supranuclear Palsy, Progressive, 1
MIP
Severe Acute Respiratory Syndrome
Cataract 41
NHS
Bloodstream Infections
Cataract 41