DISEASES

Disease-gene associations mined from literature

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Human genes for combined oxidative phosphorylation deficiency 19

Combined oxidative phosphorylation deficiency 19 [DOID:0111476]

A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in LYRM4 on chromosome 6p25.1.

Synonyms:  combined oxidative phosphorylation deficiency 19,  DOID:0111476,  COXPD19,  severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency,  severe neonatal lactic acidosis due to NFS1ISD11 complex deficiency

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.