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Diseases
Genes (754)
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TTPA
Familial Isolated Vitamin E Deficiency
Nyctalopia
GM2A
Gm2-Gangliosidosis, Ab Variant
APRT
Adenine Phosphoribosyltransferase Deficiency
PCCA
Propionic Acidemia
PCCB
Propionic Acidemia
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
HOGA1
Primary Hyperoxaluria Type 3
PDGFRB
Primary Familial Brain Calcification
MMAA
Methylmalonic Aciduria, Cbla Type
PRPS1
Phosphoribosylpyrophosphate Synthetase Superactivity
IFIH1
Singleton Merten Syndrome
TNF
Callosity
Listeriosis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
ASS1
Citrullinemia Type I
PDGFB
Callosity
Primary Familial Brain Calcification
RB1
Pinealoblastoma
Trilateral Retinoblastoma
NRL
Nyctalopia
NYX
Nyctalopia
SOST
Callosity
Craniodiaphyseal Dysplasia