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Diseases
Genes (1754)
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SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
MAGEL2
Prader–willi Syndrome
CREBBP
Chromosome 16p13.3 Deletion Syndrome, Proximal
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
SNRPN
Prader–willi Syndrome
SS18
Synovial Sarcoma
KRT17
Pachyonychia Congenita
Keratoacanthoma
NDN
Prader–willi Syndrome
EP300
Synovial Sarcoma
Ankylosing Spondylitis
Chromosome 16p13.3 Deletion Syndrome, Proximal
KRT16
Pachyonychia Congenita
BCL2
Synovial Sarcoma
Edwards Syndrome
Primary Ovarian Insufficiency
Keratoacanthoma
HAVCR2
Ankylosing Spondylitis
Subcutaneous T-Cell Lymphoma
HLA-B
Severe Acute Respiratory Syndrome
Ankylosing Spondylitis
NR5A1
Clitoromegaly
Primary Ovarian Insufficiency
IL23R
Ankylosing Spondylitis
Salmonellosis
ANTXR2
Ankylosing Spondylitis
ERAP1
Ankylosing Spondylitis
ACE
Severe Acute Respiratory Syndrome
Synovial Sarcoma
Ankylosing Spondylitis
Primary Ovarian Insufficiency
CARD9
Ankylosing Spondylitis