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Diseases
Genes (1852)
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RET
Pheochromocytoma
Trichohepatoenteric Syndrome 1
ASL
Argininosuccinic Aciduria
Meningioma
ABCC9
Cardiomyopathy, Dilated, 1i
Cantú Syndrome
LIPA
Hypercholesterolemia
Acid Lipase Disease
MYO5B
Trichohepatoenteric Syndrome 1
Diarrhea 2, With Microvillus Atrophy
Cholestasis, Progressive Familial Intrahepatic, 1
BUB1B
Trichohepatoenteric Syndrome 1
Mosaic Variegated Aneuploidy Syndrome 1
SDHD
Pheochromocytoma
Trichohepatoenteric Syndrome 1
Meningioma
SDHB
Pheochromocytoma
Meningioma
TP53
Pheochromocytoma
Trichohepatoenteric Syndrome 1
Leukemia, Chronic Lymphocytic, Susceptibility To, 4
Fibrolamellar Hepatocellular Carcinoma
Meningioma
PMM2
Pmm2 Deficiency
VHL
Pheochromocytoma
Trichohepatoenteric Syndrome 1
Meningioma
LDLR
Cystinosis
Hypercholesterolemia
APOB
Hypercholesterolemia
MAX
Pheochromocytoma
TMEM127
Pheochromocytoma
SCARB2
Epilepsy, Progressive Myoclonic, 4, With Or Without Renal Failure
NF2
Meningioma
SLC30A10
Hypermanganesemia With Dystonia 1
APOE
Trichohepatoenteric Syndrome 1
Hypercholesterolemia
Meningioma
Cholestasis, Progressive Familial Intrahepatic, 1
GDNF
Pheochromocytoma