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Details
Link-It Detail - Disease - Fetal Growth Retardation
Debug Stats
  • ### Total Build Time: 39 ms 45.164 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 346 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 251 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 984 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.135 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 14.163 KB
  • CONCEPT_GENES gt=35 ms Completed: 35 ms rowSize= 23.949 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Fetal Growth Retardation C0015934
Definition (1)
Inhibition of fetal growth resulting in the inability of the fetus to achieve its potential size.
Semantic Types (1)
Sign or Symptom (T184)
Parents (2)
img Growth Disorders C0018273
img Fetal Diseases C0015929
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306604img Growth Disorders C0018273
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Fetal Diseases C00159293img Fetal Diseases C0015929
img Female Urogenital Diseases and Pregnancy Complications C1720765img Pregnancy Complications C00329624img Fetal Diseases C0015929
Relationships (166)

Relation Types:
diso_​to_​anat : 29
diso_​to_​chem : 12
diso_​to_​diso : 97
diso_​to_​phen : 2
diso_​to_​phys : 26


Relationships:
none : 132
associated_​with : 1
classifies : 1
isa : 2
location_​of : 1
mapped_​to : 23
use : 5
used_​for : 1
Page Size
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  Page 1 of 7
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN220img genetic aspects C0017399
DISO_to_ANAT203img Placenta C0032043
DISO_to_ANAT175img In Blood C0005768
DISO_to_DISO174img Pre-Eclampsia C0032914
DISO_to_DISO137img Pre-Eclampsia C0032914
DISO_to_ANAT136img Placenta C0032043
DISO_to_PHEN118img genetic aspects C0017399
DISO_to_DISO114img Complication Aspects C1171258
DISO_to_ANAT112img In Blood C0005768
DISO_to_DISO98img Infant, Small for Gestational Age C0021296
DISO_to_PHYS81img Fetal Development C0015928
DISO_to_PHYS80img Birth Weight C0005612
DISO_to_DISO71img DELAYED EFF PRENATAL EXPOSURE C0033054
DISO_to_DISO70img Pregnancy Complications C0032962
DISO_to_ANAT69img Structure of umbilical artery C0041632
DISO_to_DISO66img Premature Birth C0151526
DISO_to_DISO65img Infant, Small for Gestational Age C0021296
DISO_to_DISO59img chemically induced C0007994
DISO_to_ANAT58img Structure of umbilical artery C0041632
DISO_to_ANAT55img Fetus C0015965
DISO_to_DISO53img OUTCOME PREGN C0032972
DISO_to_DISO52img OUTCOME PREGN C0032972
DISO_to_DISO50img Chronic fetal deprivation syndrome C0032051
DISO_to_ANAT48img Fetus C0015965
DISO_to_PHYS48img Birth Weight C0005612
Genes (37)

Species:
human : 37
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanZFP57346171ZFP57 zinc finger protein
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanHYLS1219844hydrolethalus syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanSTOX1219736storkhead box 1
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanGFM185476G elongation factor, mitochondrial 1
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanSTRA664220stimulated by retinoic acid 6
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanHYMAI57061hydatidiform mole associated and imprinted (non-protein coding)
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanZMPSTE2410269zinc metallopeptidase STE24
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanCD9610225CD96 molecule
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanCUL79820cullin 7
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanGTF2IRD19569GTF2I repeat domain containing 1
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanYWHAE7531tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanABCC86833ATP-binding cassette, sub-family C (CFTR/MRP), member 8
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanRAPSN5913receptor-associated protein of the synapse
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanPLAGL15325pleiomorphic adenoma gene-like 1
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanPKLR5313pyruvate kinase, liver and RBC
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanPCNT5116pericentrin
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanPAFAH1B15048platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanLMNA4000lamin A/C
img OMIM, Score=1000, UMLKSK CUI: C0015934
HumanKCNJ113767potassium inwardly-rectifying channel, subfamily J, member 11
img OMIM, Score=1000, UMLKSK CUI: C0015934
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015934Fetal Growth Retardation0self