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Details
Link-It Detail - Human Phenotype - Abnormality of histidine family amino acid metabolism
Debug Stats
  • ### Total Build Time: 5 ms 6.321 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 228 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 235 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= 457 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 458 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.109 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 1.675 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.047 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of histidine family amino acid metabolism HP:0010904
Definition (1)
An abnormality of a `histidine family amino acid metabolic process` (GO:0009075).
Parents (1)
img Abnormality of amino acid metabolism HP:0004337
Children (1)
img Abnormality of histidine metabolism HP:0010905
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of amino acid metabolism HP:0004337
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of amino acid metabolism HP:0004337
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanAASS10157aminoadipate-semialdehyde synthase
HumanHAL3034histidine ammonia-lyase
img HP RolledUp, OMIM ID: 235800
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010904Abnormality of histidine family amino acid metabolism0self