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Details
Link-It Detail - Disease - Congenital lysinuria
Debug Stats
  • ### Total Build Time: 17 ms 18.287 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 7 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=13 ms Completed: 13 ms rowSize= 12.309 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 4.424 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital lysinuria C0268647
Relationships (49)

Relation Types:
diso_​to_​diso : 49


Relationships:
alias_​of : 1
isa : 3
manifestation_​of : 45
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg ATROPHY MUSCLE C0026846
DISO_to_DISOmanifestation_ofimg Abdominal Obesities C0311277
DISO_to_DISOmanifestation_ofimg Anemia C0002871
DISO_to_DISOmanifestation_ofimg Aversion to protein-rich food C2673720
DISO_to_DISOmanifestation_ofimg Bone marrow may show hemophagocytosis C2673727
DISO_to_DISOmanifestation_ofimg CKD - Chronic Kidney Disease C1561643
DISO_to_DISOmanifestation_ofimg Caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene (SLC7A7, 603593.0001) C2673729
DISO_to_DISOmanifestation_ofimg Coma may occur after force feeding of high protein diet C2673714
DISO_to_DISOalias_ofimg Congenital lysinuria C0268647
DISO_to_DISOmanifestation_ofimg Cutis Laxa C0010495
DISO_to_DISOmanifestation_ofimg Decreased blood levels of cationic amino acids C2673724
DISO_to_DISOmanifestation_ofimg Decreased stature C2673718
DISO_to_DISOmanifestation_ofimg Diarrhea C0011991
DISO_to_DISOisaimg Dibasic aminoaciduria C0268648
DISO_to_DISOisaimg Dibasic aminoaciduria - type I C0341704
DISO_to_DISOisaimg Dibasic aminoaciduria - type II C0268651
DISO_to_DISOmanifestation_ofimg Enlarged Liver C0019209
DISO_to_DISOmanifestation_ofimg Enlarged Spleen C0038002
DISO_to_DISOmanifestation_ofimg Failure to Thrive C0015544
DISO_to_DISOmanifestation_ofimg Highly variable phenotype C1865012
DISO_to_DISOmanifestation_ofimg Hyperammonemia after protein intake C2673725
DISO_to_DISOmanifestation_ofimg Hyperammonemic coma C2673735
DISO_to_DISOmanifestation_ofimg Hyperelastic skin C1866955
DISO_to_DISOmanifestation_ofimg Impaired intestinal absorption of cationic amino acids C2673721
DISO_to_DISOmanifestation_ofimg Impaired renal absorption of cationic amino acids C2673717
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
img GENERIF, Score=1000, Pubmed Id: 17666782, UMLKSK CUI: C0268647
img GENERIF, Score=1000, Pubmed Id: 15756301, UMLKSK CUI: C0268647
img GENERIF, Score=1000, Pubmed Id: 12402335, UMLKSK CUI: C0268647
img GENERIF, Score=1000, Pubmed Id: 15776427, UMLKSK CUI: C0268647
img GENERIF, Score=1000, Pubmed Id: 18716612, UMLKSK CUI: C0268647
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268647Congenital lysinuria0self