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Diseases
Genes (556)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
ASS1
Uveitis
Argininosuccinic Aciduria
Citrullinemia Type I
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
TNF
Uveitis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Tachycardia
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
VIP
Uveitis
Tachycardia
MYH11
Berdon Syndrome
DRD2
Delirium Tremens
Tachycardia
MYLK
Berdon Syndrome
CTNS
Cystinosis
RBP3
Uveitis
RB1
Pinealoblastoma
Trilateral Retinoblastoma