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Diseases
Genes (963)
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COL2A1
Collagen, Type Ii, Alpha-1
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
PAH
Phenylketonuria
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
CFH
Drusen
Membranoproliferative Glomerulonephritis
ZIC1
Craniosynostosis 1
CCDC50
Deafness, Autosomal Dominant 44
SLC1A1
Normal Tension Glaucoma
TSLP
Membranoproliferative Glomerulonephritis