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Diseases
Genes (564)
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AFG3L2
Spinocerebellar Ataxia Type 28
TTPA
Familial Isolated Vitamin E Deficiency
TFAP2A
Branchiooculofacial Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
TGM1
Bathing Suit Ichthyosis
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ZIC1
Craniosynostosis 1
CCDC50
Deafness, Autosomal Dominant 44
SLC1A1
Normal Tension Glaucoma
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis