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Diseases
Genes (869)
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ABHD5
Cerebral Creatine Deficiency
WRN
Werner Syndrome
DYSF
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PITX3
Anterior Segment Dysgenesis 1
IFIH1
Hepatitis E
Singleton Merten Syndrome
PIGA
Paroxysmal Nocturnal Hemoglobinuria 1
XDH
Hyperuricemia
FOXE3
Anterior Segment Dysgenesis 1
STX3
Microvillus Inclusion Disease
HPRT1
Hyperuricemia
Paroxysmal Nocturnal Hemoglobinuria 1
ABCG2
Hyperuricemia
SLC2A9
Hyperuricemia
CD59
Paroxysmal Nocturnal Hemoglobinuria 1
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
Hyperuricemia
PIGT
Paroxysmal Nocturnal Hemoglobinuria 1
PXDN
Anterior Segment Dysgenesis 1