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Diseases
Genes (1278)
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TTPA
Neurological Disorder
Familial Isolated Vitamin E Deficiency
FMR1
Neurological Disorder
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Fg Syndrome
POLG
Neurological Disorder
Balo Concentric Sclerosis
SLC12A6
Neurological Disorder
Andermann Syndrome
PQBP1
Neurological Disorder
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC17A5
Salla Disease
NGLY1
Ngly1 Deficiency
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
Citrullinemia Type I
MSX1
Anodontia
MYH11
Berdon Syndrome
MYLK
Neurological Disorder
Berdon Syndrome
TNF
Neurological Disorder
Contrast-Induced Nephropathy
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Anodontia
Salla Disease