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Diseases
Genes (816)
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COL1A1
Osteogenesis Imperfecta Type Iv
Osteogenesis Imperfecta Type I
COL1A2
Osteogenesis Imperfecta Type Iv
Osteogenesis Imperfecta Type I
HGD
Alkaptonuria
Ochronosis
IKBKG
Melanism
Klippel-Trenaunay-Weber Syndrome
Incontinentia Pigmenti
MTOR
Gray Matter Heterotopia
Isolated Focal Cortical Dysplasia
ADGRG1
Bilateral Frontoparietal Polymicrogyria
COL4A1
Schizencephaly
TSC1
Isolated Focal Cortical Dysplasia
TSC2
Isolated Focal Cortical Dysplasia
SPARC
Osteogenesis Imperfecta Type Iv
Osteogenesis Imperfecta Type I
CRTAP
Osteogenesis Imperfecta Type Iv
Osteogenesis Imperfecta Type I
AGGF1
Klippel-Trenaunay-Weber Syndrome
SIX3
Schizencephaly
IDH2
Oligodendroglioma
CRYAA
Nuclear Sclerosis
EMX2
Schizencephaly
WNT1
Osteogenesis Imperfecta Type Iv
Schizencephaly
GJA8
Nuclear Sclerosis
SOST
Craniodiaphyseal Dysplasia
Callosity
Klippel-Trenaunay-Weber Syndrome
Osteogenesis Imperfecta Type I
SHH
Schizencephaly