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Diseases
Genes (405)
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PRNP
Kuru, Susceptibility To
Transmissible Spongiform Encephalopathy
COL2A1
Collagen, Type Ii, Alpha-1
PQBP1
Renpenning's Syndrome
SLC4A1
Southeast Asian Ovalocytosis
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
SRD5A2
5α-Reductase Deficiency
PAH
Phenylketonuria
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ITGB3
Coronary Thrombosis
SLC11A1
Buruli Ulcer
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification
DDX58
Singleton Merten Syndrome
PLAT
Coronary Thrombosis
PRSS56
Cystic Eyeball