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Diseases
Genes (1282)
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BRAF
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Retinoblastoma
Erdheim–chester Disease
RB1
Pinealoblastoma
Trilateral Retinoblastoma
Retinoblastoma
PMM2
Pmm2 Deficiency
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
GLMN
Glomuvenous Malformation
KRAS
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Retinoblastoma
Melorheostosis
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
TEK
Glomuvenous Malformation
Multiple Cutaneous And Mucosal Venous Malformations
DNAJC19
3-Methylglutaconic Aciduria, Type V
TP53
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Retinoblastoma
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
NF1
Pilocytic Astrocytoma
Retinoblastoma
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
Retinoblastoma
MYH11
Berdon Syndrome