Mitochondrial inheritance
Symptom Information:
| Symptom ID: | HPO:0001427 | ||
| Synonyms: |
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| Quality: | |||
| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Mode of inheritance(HPO:0000005) Mitochondrial inheritance(HPO:0001427) MedDRA: |
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| Database Frequency: | 12 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| COMPLEX I, SUBUNIT ND2 | (OMIM:516001) |
| COMPLEX I, SUBUNIT ND5 | (OMIM:516005) |
| COMPLEX I, SUBUNIT ND6 | (OMIM:516006) |
| COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I | (OMIM:516030) |
| CYCLIC VOMITING SYNDROME | (OMIM:500007) |
| CYTOCHROME b OF COMPLEX III | (OMIM:516020) |
| CYTOCHROME c OXIDASE III | (OMIM:516050) |
| Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect | (Orphanet:280671) |
| MYOGLOBINURIA, RECURRENT | (OMIM:550500) |
| Mitochondrial nonsyndromic sensorineural deafness | (Orphanet:90641) |
| ONCOCYTOMA | (OMIM:553000) |
| Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |