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Disease table of MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3
OMIM ID: 614053
Gene-disease associations table
Gene
Associated with MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3 in
Link to HGNC
Cytogenetic band
Number of associated diseases
Associated diseases
ATP5E
ClinVar, OMIM, HUMSAVAR
HGNC link
20q13.32
1
614053
Download the disease annotation in CSV format