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Diseases
Genes (1285)
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TTPA
Familial Isolated Vitamin E Deficiency
Metamorphopsia
ATP13A2
Kufor–rakeb Syndrome
Dementia
ITM2B
Retinal Dystrophy With Inner Retinal Dysfunction And Ganglion Cell Abnormalities
Dementia
PQBP1
Pectus Excavatum
Renpenning's Syndrome
ADA2
Sneddon Syndrome
Dementia
FAM20A
Enamel-Renal Syndrome
ACVR2B
Heterotaxy, Visceral, 7, Autosomal
TREM2
Dementia
APP
Dementia
IFIH1
Singleton Merten Syndrome
MMP21
Heterotaxy, Visceral, 7, Autosomal
NOTCH3
Pectus Excavatum
Dementia
ZIC3
Heterotaxy, Visceral, 7, Autosomal
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
LEFTY2
Heterotaxy, Visceral, 7, Autosomal
MAPT
Dementia
PRNP
Dementia
GRN
Dementia
PSEN2
Dementia