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Diseases
Genes (1034)
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MYO15A
Deafness, Autosomal Recessive 3
TTPA
Familial Isolated Vitamin E Deficiency
TFAP2A
Branchiooculofacial Syndrome
PIK3CD
Tonsil Carcinoma
Leiomyoma, Uterine
Activated Pi3k Delta Syndrome
UMOD
Medullary Cystic Kidney Disease
PQBP1
Renpenning's Syndrome
PDGFRB
Primary Familial Brain Calcification
Leiomyoma, Uterine
PHKG2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
SLC20A2
Primary Familial Brain Calcification
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
Leiomyoma, Uterine
IFIH1
Singleton Merten Syndrome
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
ZIC1
Craniosynostosis 1
CCDC50
Deafness, Autosomal Dominant 44
TSC2
Leiomyoma, Uterine
GRIN2A
Rolandic Epilepsy
SLC1A1
Normal Tension Glaucoma
PDGFB
Primary Familial Brain Calcification
HMGA2
Leiomyoma, Uterine