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Details
Link-It Detail - Human Phenotype - Abnormal mitochondrial morphology
Debug Stats
  • ### Total Build Time: 9 ms 9.192 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 197 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 795 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 783 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.990 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 2.094 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal mitochondrial morphology HP:0008322
Definition (1)
Any structural anomaly of the mitochondria.
Parents (2)
img Abnormality of the mitochondrion HP:0012103
img Abnormality of mitochondrial metabolism HP:0003287
Children (2)
img Abnormal mitochondrial number HP:0012102
img Abnormal mitochondrial shape HP:0012087
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the mitochondrion HP:0012103
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of mitochondrial metabolism HP:0003287
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of mitochondrial metabolism HP:0003287
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of mitochondrial metabolism HP:0003287
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanTAZ6901tafazzin
img HP IEA, OMIM ID: 302060
HumanSLC25A35250solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3
img HP RolledUp, OMIM ID: 610773
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0008322Abnormal mitochondrial morphology0self