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Diseases
Genes (1554)
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TRNL1
Mitochondrial Encephalomyopathy
Merrf Syndrome
ASL
Argininosuccinic Aciduria
SCN5A
Cardiac Conduction Defect
PMM2
Pmm2 Deficiency
HAMP
Anemia
Iron Deficiency Anemia
FKRP
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
SLC52A3
Brown-Vialetto-Van Laere Syndrome 1
MED12
Fg Syndrome
MFSD8
Macular Dystrophy With Central Cone Involvement
POMGNT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
POMT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
DAG1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
CRPPA
Anemia
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
FKTN
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
SOD2
Merrf Syndrome
Anemia
Mesothelioma, Malignant
POMGNT2
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
B4GAT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
CDKN2A
Anemia
Mesothelioma, Malignant