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Diseases
Genes (781)
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ATP7B
Wilson's Disease
TTPA
Familial Isolated Vitamin E Deficiency
TNF
Normal Tension Glaucoma
Oral Submucous Fibrosis
Wilson's Disease
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
TFAP2A
Branchiooculofacial Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
PQBP1
Renpenning's Syndrome
IL6
Normal Tension Glaucoma
Oral Submucous Fibrosis
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
LOX
Oral Submucous Fibrosis
Wilson's Disease
TIMP1
Oral Submucous Fibrosis
Wilson's Disease
Pleural Effusion
CXCL8
Normal Tension Glaucoma
Oral Submucous Fibrosis
Wilson's Disease
CCDC50
Deafness, Autosomal Dominant 44
SLITRK1
Trichotillomania
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome