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Details
Link-It Detail - Disease - Hyperornithinemia
Debug Stats
  • ### Total Build Time: 59 ms 7.691 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 329 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=1 ms Completed: 1 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= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=28 ms Completed: 28 ms rowSize= 3.033 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 2.791 KB
  • CONCEPT_XREFS gt=11 ms Completed: 11 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Disease (1)
Hyperornithinemia C0599035
Definition (1)
excess of ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperamonemia-homocitrullinuria syndrome.
Relationships (5)

Relation Types:
diso_​to_​chem : 1
diso_​to_​diso : 4


Relationships:
associated_​with : 2
isa : 1
use : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEMassociated_withimg Ornithine-Oxo-Acid Transaminase C0029278
DISO_to_DISOassociated_withimg 270 CONGENITAL DEFICIENCIES C0333006
DISO_to_DISOuseimg Gyrate Atrophy C0018425
DISO_to_DISOisaimg HHH C0268540
DISO_to_DISOuseimg Hyperornithinemia C0599035
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
img GENERIF, Score=1000, Pubmed Id: 11668643, UMLKSK CUI: C0599035
img GENERIF, Score=1000, Pubmed Id: 14759633, UMLKSK CUI: C0599035
img OMIM, Score=1000, UMLKSK CUI: C0599035
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0599035Hyperornithinemia0self