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Diseases
Genes (557)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Hartnup Disease
TFAP2A
Branchiooculofacial Syndrome
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
IFIH1
Singleton Merten Syndrome
ZIC1
Craniosynostosis 1
SLITRK1
Trichotillomania
CCDC50
Deafness, Autosomal Dominant 44
SLC1A1
Normal Tension Glaucoma
PDGFB
Primary Familial Brain Calcification
ASS1
Citrullinemia Type I
HOXB8
Trichotillomania
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma