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Diseases
Genes (967)
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RB1
Pinealoblastoma
Retinoblastoma
Trilateral Retinoblastoma
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
ASS1
Argininosuccinic Aciduria
Retinoblastoma
Citrullinemia Type I
SYCP3
Spermatogenesis Arrest
MDM4
Retinoblastoma
CST3
Cerebral Amyloid Angiopathy
DDX58
Singleton Merten Syndrome
KDM3B
Metal Toxicity
BCOR
Retinoblastoma
FH
Fumarase Deficiency
PTPN22
Giant Cell Arteritis
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
FLNA
Intestinal Neuronal Dysplasia
KDR
Retinoblastoma
Lathyrism