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Diseases
Genes (1047)
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CLN6
Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive
Ceroid Lipofuscinosis, Neuronal, 6
TPP1
Merrf Syndrome
Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive
Ceroid Lipofuscinosis, Neuronal, 6
SLC52A3
Brown-Vialetto-Van Laere Syndrome 2
Multiple Acyl-Coa Dehydrogenase Deficiency
Fazio-Londe Disease
ABHD5
Cerebral Creatine Deficiency
RET
Pheochromocytoma
CLN3
Merrf Syndrome
Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive
Ceroid Lipofuscinosis, Neuronal, 6
ACADM
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of
GAMT
Guanidinoacetate Methyltransferase Deficiency
JAG1
Alagille Syndrome 2
TP53
Pheochromocytoma
Alopecia, Androgenetic, 1
Brainstem Glioma
Leukemia, Chronic Lymphocytic, Susceptibility To, 5
MAX
Pheochromocytoma
VHL
Pheochromocytoma
TMEM127
Pheochromocytoma
SDHB
Pheochromocytoma
SDHD
Pheochromocytoma
ETFDH
Cerebral Creatine Deficiency
Multiple Acyl-Coa Dehydrogenase Deficiency
SLC25A20
Carnitine-Acylcarnitine Translocase Deficiency
Multiple Acyl-Coa Dehydrogenase Deficiency
ABCC9
Cantú Syndrome
ETFA
Cerebral Creatine Deficiency
Multiple Acyl-Coa Dehydrogenase Deficiency
SLC2A10
Arterial Tortuosity Syndrome