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Diseases
Genes (1050)
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TBX5
Holt–oram Syndrome
IFIH1
Singleton Merten Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
PDGFB
Primary Familial Brain Calcification
KLK3
Benign Prostatic Hyperplasia (Bph)
SRD5A2
Benign Prostatic Hyperplasia (Bph)
ITGB3
Coronary Thrombosis
DDX58
Singleton Merten Syndrome
LEMD3
Melorheostosis
CNNM2
Tetany
SALL4
Holt–oram Syndrome
PLAT
Coronary Thrombosis
CST1
Hay Fever
FGF7
Benign Prostatic Hyperplasia (Bph)
PRL
Benign Prostatic Hyperplasia (Bph)
NPY
Nasal Congestion
RSPH4A
Nasal Congestion
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification