MT-ND3 - Gene browser

MT-ND3

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3

HCNC Approved Symbol: MT-ND3 (HGNC:7458)
Genomic Coordinates: -:- - - (mitochondria)
Synonyms: ND3, NAD3, MTND3
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.

6Patients

In total, 6 patients were diagnosed with a variant in the MT-ND3 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

06
Patient count

Seizures: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Increased serum pyruvate: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Strabismus: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Cerebral gyral anomalies: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Divergent strabismus: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)