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Details
Link-It Detail - Disease - Rhabdomyolysis
Debug Stats
  • ### Total Build Time: 40 ms 35.273 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=1 ms Completed: 1 ms rowSize= 211 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= 232 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 553 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 551 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.781 KB
  • CONCEPT_RELATIONSHIPS gt=24 ms Completed: 24 ms rowSize= 13.075 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 16.412 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Rhabdomyolysis C0035410
Definition (1)
a potentially fatal disease that destroys skeletal muscle
Semantic Types (2)
Pathologic Function (T046)
Finding (T033)
Parents (1)
img Muscular Diseases C0026848
Children (1)
img Myoglobinuria C0027080
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neuromuscular Diseases C00278684img Muscular Diseases C0026848
img Musculoskeletal Diseases C0026857img Muscular Diseases C00268483img Muscular Diseases C0026848
Relationships (93)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 33
diso_​to_​diso : 48
diso_​to_​phen : 3
diso_​to_​phys : 4


Relationships:
none : 83
classifies : 1
isa : 6
mapped_​to : 3
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO287img chemically induced C0007994
DISO_to_DISO279img chemically induced C0007994
DISO_to_DISO137img Acute kidney injury C2609414
DISO_to_DISO122img Complication Aspects C1171258
DISO_to_DISO105img Acute kidney injury C2609414
DISO_to_DISO98img Complication Aspects C1171258
DISO_to_CHEM91img Hydroxymethylglutaryl-CoA Reductase Inhibitors C0360714
DISO_to_CHEM82img Hydroxymethylglutaryl-CoA Reductase Inhibitors C0360714
DISO_to_ANAT64img In Blood C0005768
DISO_to_ANAT52img In Blood C0005768
DISO_to_CHEM49img SIMVASTATIN C0074554
DISO_to_CHEM46img SIMVASTATIN C0074554
DISO_to_CHEM38img Hypolipidemic Agents C0086440
DISO_to_PHEN33img genetic aspects C0017399
DISO_to_ANAT32img Muscle, Skeletal C0242692
DISO_to_ANAT31img Muscle, Skeletal C0242692
DISO_to_CHEM31img Agents, Anticholesteremic C0003277
DISO_to_CHEM28img Pyridines C0034255
DISO_to_PHYS25img Effort, Physical C0031807
DISO_to_DISO23img Disease, Equine C0019940
DISO_to_DISO22img Hypokalemia C0020621
DISO_to_CHEM21img Hypolipidemic Agents C0086440
DISO_to_DISO21img COMPL POSTOP C0032787
DISO_to_CHEM20img Agents, Anticholesteremic C0003277
DISO_to_DISO20img Compartment Syndromes C0009492
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanUQCRQ27089ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanLPIN123175lipin 1
img GENERIF, Score=861, Pubmed Id: 18817903, UMLKSK CUI: C0035410
HumanTSFM10102Ts translation elongation factor, mitochondrial
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanCTDP19150CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanUQCRB7381ubiquinol-cytochrome c reductase binding protein
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanRYR16261ryanodine receptor 1 (skeletal)
img GENERIF, Score=827, Pubmed Id: 12066726, UMLKSK CUI: C0035410
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanPYGM5837phosphorylase, glycogen, muscle
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanPOLG5428polymerase (DNA directed), gamma
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanPGK15230phosphoglycerate kinase 1
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanHADHB3032hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanHADHA3030hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanCPT21376carnitine palmitoyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0035410
img GENERIF, Score=1000, Pubmed Id: 17709715, UMLKSK CUI: C0035410
HumanCACNA1S779calcium channel, voltage-dependent, L type, alpha 1S subunit
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanBCS1L617BC1 (ubiquinol-cytochrome c reductase) synthesis-like
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanSLC25A4291solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
img OMIM, Score=1000, UMLKSK CUI: C0035410
HumanACADVL37acyl-CoA dehydrogenase, very long chain
img OMIM, Score=1000, UMLKSK CUI: C0035410
img OMIM, Score=1000, UMLKSK CUI: C0035410
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0035410Rhabdomyolysis0self