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Diseases
Genes (1768)
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ASL
Argininosuccinic Aciduria
Meningioma
GJA1
Meningioma
Oculodentodigital Dysplasia
FOXP3
Ipex Syndrome
Lymphoma, Hodgkin, Classic
CACNA1A
Spinocerebellar Ataxia Type 6
DES
Myopathy, Myofibrillar, 1
F12
Factor Xii Deficiency
PMM2
Pmm2 Deficiency
JAK2
Thrombocythemia 3
Meningioma
Lymphoma, Hodgkin, Classic
DICER1
Pleuropulmonary Blastoma
Lymphoma, Hodgkin, Classic
NF2
Meningioma
AKT1
Thrombocythemia 3
Meningioma
Membranoproliferative Glomerulonephritis
Lymphoma, Hodgkin, Classic
SMPD1
Niemann-Pick Disease, Type B
PDGFB
Thrombocythemia 3
Meningioma
FHL1
Myopathy, X-Linked, With Postural Muscle Atrophy
RHBDF2
Meningioma
Howel–evans Syndrome
SUFU
Meningioma
Oculodentodigital Dysplasia
APOA1
Amyloidosis, Familial Visceral
Thrombocythemia 3
Meningioma
Primary Aldosteronism
B2M
Amyloidosis, Familial Visceral
Lymphoma, Hodgkin, Classic
FGA
Amyloidosis, Familial Visceral
LYZ
Amyloidosis, Familial Visceral