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Diseases
Genes (1218)
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TTPA
Neurological Disorder
Familial Isolated Vitamin E Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
PQBP1
Neurological Disorder
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
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
PAH
Phenylketonuria
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
Diverticulum
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Anodontia
BDNF
Neurological Disorder
GFAP
Neurological Disorder