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Diseases
Genes (156)
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MYO15A
Deafness, Autosomal Recessive 3
SLC6A19
Hartnup Disease
PIK3CD
Activated Pi3k Delta Syndrome
PHKG2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
PDGFB
Primary Familial Brain Calcification
PHKA2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CNNM2
Tetany
PIK3R1
Activated Pi3k Delta Syndrome
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification
PTEN
Activated Pi3k Delta Syndrome
AKAP5
Tetany
PRSS56
Cystic Eyeball
CCL11
Allergic Conjunctivitis
IFNG
Allergic Conjunctivitis
CCL5
Allergic Conjunctivitis
IRF1
Allergic Conjunctivitis