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Diseases
Genes (1646)
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TRNL1
Maternally Inherited Diabetes And Deafness
Myoclonic Epilepsy With Ragged-Red Fibers
TTPA
Familial Isolated Vitamin E Deficiency
TTN
Myopathy, Myofibrillar, 9, With Early Respiratory Failure
TRNK
Maternally Inherited Diabetes And Deafness
Myoclonic Epilepsy With Ragged-Red Fibers
ABL1
Chronic Myelogenous Leukemia
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
BCR
Chronic Myelogenous Leukemia
IFIH1
Singleton Merten Syndrome
TRNP
Myoclonic Epilepsy With Ragged-Red Fibers
TRNF
Myoclonic Epilepsy With Ragged-Red Fibers
PTEN
Thrombophlebitis
Adenoid Cystic Carcinoma
Protein Losing Enteropathy
Chronic Myelogenous Leukemia
Familial Multiple Lipomatosis
TYMP
Mitochondrial Neurogastrointestinal Encephalomyopathy
TP53
Adenoid Cystic Carcinoma
Chronic Myelogenous Leukemia
CD55
Protein Losing Enteropathy
Chronic Myelogenous Leukemia
ASS1
Chronic Myelogenous Leukemia
Citrullinemia Type I
PIK3CA
Adenoid Cystic Carcinoma
Chronic Myelogenous Leukemia
JAK2
Thalassemia
Chronic Myelogenous Leukemia
SETBP1
Chronic Myelogenous Leukemia
NOTCH1
Adenoid Cystic Carcinoma
Chronic Myelogenous Leukemia