COMPLEX I, SUBUNIT ND5

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr:
OMIM Id: 516005
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0001085) Papilledema 31 / 7739
2
 (HPO:0000543) Optic disc pallor 67 / 7739
3
 (HPO:0001117) Sudden loss of visual acuity 6 / 7739
4
 (HPO:0001129) Large central visual field defect 6 / 7739
5
 (HPO:0001112) Leber optic atrophy 9 / 7739
6
 (HPO:0002315) Headache 175 / 7739
7
 (HPO:0001939) Abnormality of metabolism/homeostasis 328 / 7739
8
 (HPO:0003674) Onset 32 / 7739
9
 (HPO:0001427) Mitochondrial inheritance 12 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: