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Details
Link-It Detail - Disease - Protein Deficiency
Debug Stats
  • ### Total Build Time: 104 ms 26.394 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 849 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 565 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.520 KB
  • CONCEPT_RELATIONSHIPS gt=80 ms Completed: 80 ms rowSize= 12.610 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 8.651 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Protein Deficiency C0033626
Definition (1)
A nutritional condition produced by a deficiency of proteins in the diet, characterized by adaptive enzyme changes in the liver, increase in amino acid synthetases, and diminution of urea formation, thus conserving nitrogen and reducing its loss in the urine. Growth, immune response, repair, and production of enzymes and hormones are all impaired in severe protein deficiency. Protein deficiency may also arise in the face of adequate protein intake if the protein is of poor quality (i.e., the content of one or more amino acids is inadequate and thus becomes the limiting factor in protein utilization). (From Merck Manual, 16th ed; Harrison's Principles of Internal Medicine, 12th ed, p406)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Deficiency Diseases C0011156
Children (1)
img Protein-Energy Malnutrition C0033677
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Nutrition Disorders C00287095img Deficiency Diseases C0011156
Relationships (65)

Relation Types:
diso_​to_​anat : 9
diso_​to_​chem : 42
diso_​to_​diso : 8
diso_​to_​phen : 1
diso_​to_​phys : 5


Relationships:
none : 28
entry_​version_​of : 1
may_​treat : 36
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO29img Complication Aspects C1171258
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_CHEM16img Dietary Proteins C0012177
DISO_to_DISO13img Prenatal Exposure Delayed Effects C0033054
DISO_to_CHEM12img Dietary Protein C0012177
DISO_to_DISO10img DELAYED EFF PRENATAL EXPOSURE C0033054
DISO_to_ANAT8img In Blood C0005768
DISO_to_ANAT8img Liver C0023884
DISO_to_ANAT7img Liver C0023884
DISO_to_ANAT6img Neurons C0027882
DISO_to_DISO6img Malnutrition C0162429
DISO_to_DISO6img Pregnancy Complications C0032962
DISO_to_PHEN6img genetic aspects C0017399
DISO_to_PHYS6img Aging C0001811
DISO_to_ANAT5img Brain C0006104
DISO_to_ANAT5img Myenteric Plexus C0027028
DISO_to_ANAT5img Neurons C0027882
DISO_to_CHEM5img Antioxidants C0003402
DISO_to_PHYS5img Maternal Nutritional Physiological Phenomena C1720845
DISO_to_ANAT4img In Blood C0005768
DISO_to_ANAT4img Islets of Langerhans C0022131
DISO_to_CHEM4img Amino Acids C0002520
DISO_to_CHEM4img Insulin C0021641
DISO_to_CHEM4img Zinc C0043481
DISO_to_DISO4img Fetal Nutrition Disorders C1285261
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
img OMIM, Score=1000, UMLKSK CUI: C0033626
HumanPROZ8858protein Z, vitamin K-dependent plasma glycoprotein
img GENERIF, Score=913, Pubmed Id: 17701666, UMLKSK CUI: C0033626
img GENERIF, Score=913, Pubmed Id: 15314579, UMLKSK CUI: C0033626
HumanSHBG6462sex hormone-binding globulin
INFERRED, Score=800, UMLKSK CUI: C0033626
HumanSLC25A35250solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3
img GENERIF, Score=901, Pubmed Id: 17273968, UMLKSK CUI: C0033626
HumanLEPR3953leptin receptor
INFERRED, Score=800, UMLKSK CUI: C0033626
HumanEPB422038erythrocyte membrane protein band 4.2
img GENERIF, Score=875, Pubmed Id: 12393467, UMLKSK CUI: C0033626
HumanCD47961CD47 molecule
img GENERIF, Score=875, Pubmed Id: 12393467, UMLKSK CUI: C0033626
HumanABCD1215ATP-binding cassette, sub-family D (ALD), member 1
img GENERIF, Score=901, Pubmed Id: 15772093, UMLKSK CUI: C0033626
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0033626Protein Deficiency0self