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Diseases
Genes (2204)
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TRNL1
Maternally Inherited Diabetes And Deafness
Myoclonic Epilepsy With Ragged-Red Fibers
BRAF
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Cryptorchidism
Pleomorphic Xanthoastrocytoma
Chronic Myelogenous Leukemia
TTPA
Familial Isolated Vitamin E Deficiency
KRAS
Pilocytic Astrocytoma
Intraductal Papillary Mucinous Neoplasm
Cryptorchidism
Pleomorphic Xanthoastrocytoma
Chronic Myelogenous Leukemia
INSL3
Cryptorchidism
ABL1
Cryptorchidism
Chronic Myelogenous Leukemia
GLMN
Glomuvenous Malformation
DNAJC19
3-Methylglutaconic Aciduria, Type V
Cryptorchidism
TTN
Myopathy, Myofibrillar, 9, With Early Respiratory Failure
TRNK
Maternally Inherited Diabetes And Deafness
Myoclonic Epilepsy With Ragged-Red Fibers
PQBP1
Renpenning's Syndrome
TEK
Glomuvenous Malformation
Multiple Cutaneous And Mucosal Venous Malformations
Chronic Myelogenous Leukemia
BCR
Chronic Myelogenous Leukemia
IFIH1
Singleton Merten Syndrome
TRNP
Myoclonic Epilepsy With Ragged-Red Fibers
TRNF
Myoclonic Epilepsy With Ragged-Red Fibers
NF1
Fibrous Dysplasia Of Bone
Pilocytic Astrocytoma
Cryptorchidism
Chronic Myelogenous Leukemia
ESR1
Pilocytic Astrocytoma
Cryptorchidism
Chronic Myelogenous Leukemia
FGFR1
Pilocytic Astrocytoma
Cryptorchidism
Chronic Myelogenous Leukemia
TYMP
Mitochondrial Neurogastrointestinal Encephalomyopathy