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Diseases
Genes (1110)
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FGFR3
Muenke Syndrome
Tonsil Carcinoma
Craniosynostosis 1
AGL
Glycogen Storage Disease Iii
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
EDN1
Auriculocondylar Syndrome 3
Membranoproliferative Glomerulonephritis
Normal Tension Glaucoma
TFAP2A
Branchiooculofacial Syndrome
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
CFH
Drusen
Membranoproliferative Glomerulonephritis
Pleural Effusion
GALE
Galactose Epimerase Deficiency
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
IFIH1
Singleton Merten Syndrome
ZIC1
Craniosynostosis 1
CCDC50
Deafness, Autosomal Dominant 44
SLC1A1
Normal Tension Glaucoma
TSLP
Membranoproliferative Glomerulonephritis
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis