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Diseases
Genes (481)
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ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
ASS1
Uveitis
Argininosuccinic Aciduria
Citrullinemia Type I
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
RBP3
Uveitis
MRAP
Uveitis
Familial Glucocorticoid Deficiency
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TNF
Uveitis
Lumbar Disc Disease
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
SERPINF1
Uveitis
IL6
Uveitis
Argininosuccinic Aciduria
Lumbar Disc Disease
Familial Isolated Vitamin E Deficiency
HSPA9
Uveitis
CALB2
Uveitis
ALB
Uveitis