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Diseases
Genes (570)
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BRAF
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Erdheim–chester Disease
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GLMN
Glomuvenous Malformation
PQBP1
Renpenning's Syndrome
KRAS
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Melorheostosis
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
TEK
Glomuvenous Malformation
Multiple Cutaneous And Mucosal Venous Malformations
DNAJC19
3-Methylglutaconic Aciduria, Type V
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
NF1
Pilocytic Astrocytoma
TP53
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome