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Diseases
Genes (621)
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TTPA
Familial Isolated Vitamin E Deficiency
TFAP2A
Branchiooculofacial Syndrome
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
IFIH1
Singleton Merten Syndrome
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
TNF
Normal Tension Glaucoma
Oral Submucous Fibrosis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
ZIC1
Craniosynostosis 1
CCDC50
Deafness, Autosomal Dominant 44
SLC1A1
Normal Tension Glaucoma
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
IL6
Normal Tension Glaucoma
Oral Submucous Fibrosis
Familial Isolated Vitamin E Deficiency
Pleural Effusion
RB1
Pinealoblastoma
Trilateral Retinoblastoma
FGFR2
Oral Submucous Fibrosis
Craniosynostosis 1