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Diseases
Genes (736)
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TTPA
Familial Isolated Vitamin E Deficiency
Nyctalopia
GM2A
Gm2-Gangliosidosis, Ab Variant
TMC6
Epidermodysplasia Verruciformis
PCCA
Propionic Acidemia
PCCB
Propionic Acidemia
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
IFIH1
Dengue Fever
Singleton Merten Syndrome
PDGFRB
Primary Familial Brain Calcification
MMAA
Methylmalonic Aciduria, Cbla Type
PRPS1
Phosphoribosylpyrophosphate Synthetase Superactivity
TMC8
Epidermodysplasia Verruciformis
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CD209
Dengue Fever
NRL
Nyctalopia
DDX58
Dengue Fever
Singleton Merten Syndrome
NYX
Nyctalopia