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Diseases
Genes (1378)
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TTPA
Neurological Disorder
Familial Isolated Vitamin E Deficiency
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
PQBP1
Neurological Disorder
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
FLNA
Neurological Disorder
Intestinal Neuronal Dysplasia
Anodontia
Fg Syndrome
ACTG2
Berdon Syndrome
DSG1
Palmoplantar Keratoderma I, Striate, Focal, Or Diffuse
DMPK
Myotonic Dystrophy
CTNS
Recurrent Corneal Erosion
Cystinosis
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
MSX1
Anodontia
MYH11
Berdon Syndrome
TNF
Hepatitis E
Neurological Disorder
Contrast-Induced Nephropathy
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Myotonic Dystrophy
Anodontia
MYLK
Neurological Disorder
Berdon Syndrome
SYCP3
Spermatogenesis Arrest