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Diseases
Genes (1836)
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ALX4
Enlarged Parietal Foramina
Isolated Scaphocephaly
Isolated Oxycephaly
TWIST1
Enlarged Parietal Foramina
Isolated Scaphocephaly
Isolated Oxycephaly
Baller–gerold Syndrome
SALL4
Convergence Insufficiency
Duane-Radial Ray Syndrome
GJA1
Sepsis
Oculodentodigital Dysplasia
MMUT
Sepsis
Methylmalonyl-Coa Mutase Deficiency
COL6A1
Bethlem Myopathy
FGFR2
Enlarged Parietal Foramina
Double Outlet Right Ventricle
Isolated Scaphocephaly
Isolated Oxycephaly
MSX2
Enlarged Parietal Foramina
Isolated Scaphocephaly
ERF
Isolated Scaphocephaly
Isolated Oxycephaly
ZIC1
Isolated Scaphocephaly
Isolated Oxycephaly
SMAD6
Isolated Scaphocephaly
Isolated Oxycephaly
Coarctation Of The Aorta
IFT122
Sepsis
Anodontia
Isolated Scaphocephaly
Isolated Oxycephaly
SLC17A5
Salla Disease
COL2A1
Kniest Dysplasia
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
FGFR1
Sepsis
Anodontia
Isolated Scaphocephaly
Isolated Oxycephaly
Coarctation Of The Aorta
JAK2
Thrombocythemia
Sepsis
RECQL4
Baller–gerold Syndrome
SLC20A2
Sepsis
Primary Familial Brain Calcification