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Diseases
Genes (471)
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COL1A1
Osteogenesis Imperfecta Type I
Osteogenesis Imperfecta Type Iv
COL1A2
Osteogenesis Imperfecta Type I
Osteogenesis Imperfecta Type Iv
ABHD5
Cerebral Creatine Deficiency
IKBKG
Incontinentia Pigmenti
GAMT
Guanidinoacetate Methyltransferase Deficiency
MTOR
Gray Matter Heterotopia
Isolated Focal Cortical Dysplasia
ADGRG1
Bilateral Frontoparietal Polymicrogyria
COL4A1
Schizencephaly
TSC1
Isolated Focal Cortical Dysplasia
TSC2
Isolated Focal Cortical Dysplasia
SIX3
Schizencephaly
SPARC
Osteogenesis Imperfecta Type I
Osteogenesis Imperfecta Type Iv
CRTAP
Osteogenesis Imperfecta Type I
Osteogenesis Imperfecta Type Iv
CRYAA
Nuclear Sclerosis
EMX2
Schizencephaly
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
Incontinentia Pigmenti
GJA8
Nuclear Sclerosis
SHH
Schizencephaly
WNT1
Schizencephaly
Osteogenesis Imperfecta Type Iv