Abnormal mitochondrial shape

Symptom Information:

Symptom ID: HPO:0012087
Synonyms:
Urine color abnormality [Orphanet:38720]
Urine color abnormal (finding) [Orphanet:38720]
Discolored urine (finding) [Orphanet:38720]
Urine color abnormal [Orphanet:38720]
Abnormal colour of the urine/cholic/dark urines [Orphanet:38720]
Urine colour abnormal [Orphanet:38720]
Chromaturia [MedDRA:10008796]
Discoloration urine [MedDRA:10008796]
Red urine [MedDRA:10008796]
Urine colouring black [MedDRA:10008796]
Urine colouring yellow [MedDRA:10008796]
Urine discoloration [MedDRA:10008796]
Urine discolouration [MedDRA:10008796]
Urine coloring black [MedDRA:10008796]
Urine coloring yellow [MedDRA:10008796]
Discolouration urine [MedDRA:10008796]
Brown urine [MedDRA:10008796]
Urine colour abnormal [MedDRA:10008796]
Urine color abnormal [MedDRA:10008796]
Discoloration urine green [MedDRA:10008796]
Discolouration urine green [MedDRA:10008796]
Urine coloring green [MedDRA:10008796]
Urine colouring red [MedDRA:10008796]
Urine coloring red [MedDRA:10008796]
Urine colouring green [MedDRA:10008796]
Red urine [OMIM:Red urine]
Dark urine color [Orphanet:38720]
Urine looks dark (finding) [Orphanet:38720]
Urine looks dark [Orphanet:38720]
Quality:
Cross references:
HPO:0012086 "Abnormal urinary color" [Orphanet:38720]
Orphanet:38720 "Abnormal colour of the urine/cholic/dark urines" [Orphanet:38720]
OMIM: "Red urine" [OMIM:Red urine]
UMLS:C0522153 "Urine color abnormal" [Orphanet:38720]
UMLS:C0426396 "Urine looks dark" [Orphanet:38720]
Is a (Direct Parents):
Orphanet Abnormality of the urinary system physiology
MedDRA Urinary abnormalities
Orphanet Abnormal urinary color
HPO         Abnormal mitochondrial morphology
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)
                Abnormal mitochondrial morphology(HPO:0008322)
                   Abnormal mitochondrial shape(HPO:0012087)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary abnormalities(MedDRA:10000196)
          Abnormal mitochondrial shape(HPO:0012087)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Barth syndrome (Orphanet:111)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Cardiomyopathy-hypotonia-lactic acidosis syndrome (Orphanet:91130)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Lymphangioleiomyomatosis (Orphanet:538)
MELAS (Orphanet:550)
MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT (OMIM:254960)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)