Abnormality of the mitochondrion

Symptom Information:

Symptom ID: HPO:0012103
Synonyms:
MITOCHONDRIAL ABNORMALITIES [HPO:0012103]
Mitochondrial abnormalities [OMIM:Mitochondrial abnormalities]
Quality:
Cross references:
OMIM: "Mitochondrial abnormalities" [OMIM:Mitochondrial abnormalities]
Is a (Direct Parents):
HPO         Abnormality of cell physiology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of cell physiology(HPO:0011017)
             Abnormality of the mitochondrion(HPO:0012103)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Arrhythmogenic right ventricular dysplasia, familial, 6 (OMIM:604401)
Barth syndrome (Orphanet:111)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Combined oxidative phosphorylation defect type 13 (Orphanet:319514)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
Ramsay-Hunt syndrome (Orphanet:3020)