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Diseases
Genes (805)
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ATP7B
Wilson's Disease
TNF
Oral Submucous Fibrosis
Normal Tension Glaucoma
Wilson's Disease
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
TFAP2A
Branchiooculofacial Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
PQBP1
Renpenning's Syndrome
IL6
Oral Submucous Fibrosis
Normal Tension Glaucoma
Wilson's Disease
Pleural Effusion
Sleep Apnea
Familial Isolated Vitamin E Deficiency
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
TIMP1
Oral Submucous Fibrosis
Wilson's Disease
Pleural Effusion
LOX
Oral Submucous Fibrosis
Wilson's Disease
CXCL8
Oral Submucous Fibrosis
Normal Tension Glaucoma
Wilson's Disease
CCDC50
Deafness, Autosomal Dominant 44
ZIC1
Craniosynostosis 1
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome