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Diseases
Genes (1647)
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TRNL1
Maternally Inherited Diabetes And Deafness
Myoclonic Epilepsy With Ragged-Red Fibers
BRAF
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Chronic Myelogenous Leukemia
TTPA
Familial Isolated Vitamin E Deficiency
GLMN
Glomuvenous Malformation
TTN
Myopathy, Myofibrillar, 9, With Early Respiratory Failure
TRNK
Maternally Inherited Diabetes And Deafness
Myoclonic Epilepsy With Ragged-Red Fibers
KRAS
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Chronic Myelogenous Leukemia
ABL1
Chronic Myelogenous Leukemia
PQBP1
Renpenning's Syndrome
TEK
Glomuvenous Malformation
Multiple Cutaneous And Mucosal Venous Malformations
Chronic Myelogenous Leukemia
NF1
Fibrous Dysplasia Of Bone
Pilocytic Astrocytoma
Chronic Myelogenous Leukemia
Neurofibromatosis
DNAJC19
3-Methylglutaconic Aciduria, Type V
BCR
Chronic Myelogenous Leukemia
IFIH1
Singleton Merten Syndrome
TRNP
Myoclonic Epilepsy With Ragged-Red Fibers
TRNF
Myoclonic Epilepsy With Ragged-Red Fibers
TYMP
Mitochondrial Neurogastrointestinal Encephalomyopathy
TP53
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Pleomorphic Xanthoastrocytoma
Chronic Myelogenous Leukemia
CD55
Protein Losing Enteropathy
Chronic Myelogenous Leukemia
JAK2
Thalassemia
Chronic Myelogenous Leukemia