MT-ND5 - Gene browser

MT-ND5

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5

HCNC Approved Symbol: MT-ND5 (HGNC:7461)
Genomic Coordinates: -:- - - (mitochondria)
Synonyms: ND5, NAD5, MTND5
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.

4Patients

In total, 4 patients were diagnosed with a variant in the MT-ND5 gene.

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

04
Patient count

Developmental regression: 2 (50.0%)
Patient Count: 2 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (50.0%)
Epilepsy: 2 (50.0%)
Patient Count: 2 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (50.0%)
Persistent fetal vasculature: 1 (25.0%)
Patient Count: 1 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (25.0%)
Behavioral changes: 1 (25.0%)
Patient Count: 1 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (25.0%)
Cognitive decline: 1 (25.0%)
Patient Count: 1 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (25.0%)