Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Disease - Fetal Diseases
Debug Stats
  • ### Total Build Time: 505 ms 40.819 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 268 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 1.016 KB
  • CONCEPT_CHILDREN gt=21 ms Completed: 21 ms rowSize= 3.969 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.506 KB
  • CONCEPT_RELATIONSHIPS gt=414 ms Completed: 414 ms rowSize= 13.818 KB
  • CONCEPT_GENES gt=41 ms Completed: 41 ms rowSize= 17.571 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Fetal Diseases C0015929
Definition (1)
Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612
img Pregnancy Complications C0032962
Children (9)
img Fetal Macrosomia C0015938
img Chorioamnionitis C0008495
img Fetal Growth Retardation C0015934
img Meconium Aspiration Syndrome C0025048
img Fetal Hypoxia C0349489
img Erythroblastosis, Fetal C0014761
img Fetal Alcohol Syndrome C0015923
img Nuchal Cord C0405124
img Fetal Nutrition Disorders C1285261
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C00276122img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612
img Female Urogenital Diseases and Pregnancy Complications C1720765img Pregnancy Complications C00329623img Pregnancy Complications C0032962
Relationships (193)

Relation Types:
diso_​to_​anat : 32
diso_​to_​chem : 5
diso_​to_​diso : 149
diso_​to_​phen : 2
diso_​to_​phys : 5


Relationships:
none : 152
entry_​version_​of : 1
isa : 33
mapped_​to : 4
may_​diagnose : 1
use : 2
Page Size
Current 25
  Page 1 of 8
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN225img genetic aspects C0017399
DISO_to_PHEN202img genetic aspects C0017399
DISO_to_ANAT118img Fetus C0015965
DISO_to_ANAT103img Fetus C0015965
DISO_to_ANAT102img In Blood C0005768
DISO_to_DISO100img Pregnancy Complications C0032962
DISO_to_DISO99img Pregnancy Complications C0032962
DISO_to_DISO88img Congenital Heart Defects C0018798
DISO_to_DISO86img COMPL PREGN INFECT C0032965
DISO_to_DISO78img COMPL PREGN INFECT C0032965
DISO_to_DISO72img Abnormalities, Multiple C0000772
DISO_to_ANAT69img In Blood C0005768
DISO_to_DISO61img Congenital Abnormalities C0000768
DISO_to_DISO61img chemically induced C0007994
DISO_to_DISO60img Infant, Newborn, Diseases C0021290
DISO_to_DISO60img chemically induced C0007994
DISO_to_DISO58img Down Syndrome C0013080
DISO_to_DISO57img Heart Defects, Congenital C0018798
DISO_to_DISO57img Hernia, Diaphragmatic C0019284
DISO_to_DISO55img Congenital Abnormalities C0000768
DISO_to_DISO51img Abnormalities, Multiple C0000772
DISO_to_DISO45img Anemia C0002871
DISO_to_DISO45img OUTCOME PREGN C0032972
DISO_to_DISO43img Teratoma C0039538
DISO_to_DISO42img Diaphragmatic Hernia C0019284
Genes (72)

Species:
human : 72
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanZFP57346171ZFP57 zinc finger protein
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanHYLS1219844hydrolethalus syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanSTOX1219736storkhead box 1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanCDAN1146059codanin 1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanGFM185476G elongation factor, mitochondrial 1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanSTRA664220stimulated by retinoic acid 6
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanHYMAI57061hydatidiform mole associated and imprinted (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanALG156052ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanDEFB103B55894defensin, beta 103B
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanZMPSTE2410269zinc metallopeptidase STE24
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanCD9610225CD96 molecule
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanCUL79820cullin 7
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanYWHAE7531tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanSCGB1A17356secretoglobin, family 1A, member 1 (uteroglobin)
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0015929
HumanTLR27097toll-like receptor 2
INFERRED, Score=800, UMLKSK CUI: C0015929
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015929Fetal Diseases0self