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Diseases
Genes (1294)
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TTPA
Neurological Disorder
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
ASL
Argininosuccinic Aciduria
NGLY1
Corneal Neovascularization
Ngly1 Deficiency
PQBP1
Neurological Disorder
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
FLNA
Neurological Disorder
Intestinal Neuronal Dysplasia
Anodontia
Fg Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DSG1
Palmoplantar Keratoderma I, Striate, Focal, Or Diffuse
CTNS
Recurrent Corneal Erosion
Cystinosis
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
MSX1
Anodontia
MYH11
Berdon Syndrome
VEGFA
Neurological Disorder
Corneal Neovascularization
Lymphangiosarcoma
Erdheim–chester Disease
MYLK
Neurological Disorder
Berdon Syndrome
TNF
Neurological Disorder
Contrast-Induced Nephropathy
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Anodontia
BDNF
Neurological Disorder