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Diseases
Genes (1136)
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NAGA
Alpha-N-Acetylgalactosaminidase Deficiency
Alpha-N-Acetylgalactosaminidase Deficiency Type 3
Alpha-N-Acetylgalactosaminidase Deficiency Type 2
Infantile Neuroaxonal Dystrophy
VHL
Thrombosis
Intracranial Aneurysm
Von Hippel-Lindau Syndrome
ENG
Telangiectasia, Hereditary Hemorrhagic, Type 1
Thrombosis
Intracranial Aneurysm
ACVRL1
Telangiectasia, Hereditary Hemorrhagic, Type 1
Pulmonary Hypertension
PLA2G6
Infantile Neuroaxonal Dystrophy
Thrombosis
HIF1A
Pilocytic Astrocytoma
Intracranial Aneurysm
Von Hippel-Lindau Syndrome
Pulmonary Hypertension
GLMN
Glomuvenous Malformation
NF1
Pilocytic Astrocytoma
Fibrous Dysplasia Of Bone
Aneurysm
Intracranial Aneurysm
Neurofibromatosis
Von Hippel-Lindau Syndrome
BRAF
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Telangiectasia, Hereditary Hemorrhagic, Type 1
TTPA
Familial Isolated Vitamin E Deficiency
TNF
Intraductal Papillary Mucinous Neoplasm
Endocarditis
Thrombosis
Aneurysm
Thalassemia
Intracranial Aneurysm
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pulmonary Hypertension
MMP9
Pilocytic Astrocytoma
Enteritis
Endocarditis
Aneurysm
Intracranial Aneurysm
Pulmonary Hypertension
KRAS
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
TEK
Glomuvenous Malformation
Multiple Cutaneous And Mucosal Venous Malformations
GDF2
Telangiectasia, Hereditary Hemorrhagic, Type 1
Pulmonary Hypertension
DNAJC19
3-Methylglutaconic Aciduria, Type V
NOS3
Thrombosis
Intracranial Aneurysm
Familial Isolated Vitamin E Deficiency
Pulmonary Hypertension
PQBP1
Renpenning's Syndrome
CTC1
Cerebroretinal Microangiopathy With Calcifications And Cysts 1
HGF
Pilocytic Astrocytoma
Thrombosis
Intracranial Aneurysm