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 - Meningocele
Debug Stats
  • ### Total Build Time: 47 ms 21.634 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 320 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 294 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 979 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=7 ms Completed: 7 ms rowSize= 4.134 KB
  • CONCEPT_RELATIONSHIPS gt=27 ms Completed: 27 ms rowSize= 12.317 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 2.260 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Meningocele C0025299
Definition (1)
A congenital or acquired protrusion of the meninges, unaccompanied by neural tissue, through a bony defect in the skull or vertebral column.
Semantic Types (1)
Anatomical Abnormality (T190)
Parents (2)
img Hernia C0019270
img Neural Tube Defects C0027794
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathological Conditions, Anatomical C07521354img Hernia C0019270
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Neural Tube Defects C0027794
img Nervous System Diseases C0027765img Nervous System Malformations C04975524img Neural Tube Defects C0027794
Relationships (40)

Relation Types:
diso_​to_​anat : 9
diso_​to_​diso : 30
diso_​to_​phen : 1


Relationships:
none : 28
isa : 9
mapped_​to : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO75img Complication Aspects C1171258
DISO_to_DISO73img Congenital cerebral hernia C0014065
DISO_to_DISO70img Complication Aspects C1171258
DISO_to_DISO53img Congenital cerebral hernia C0014065
DISO_to_ANAT22img Bone structure of sacrum C0036037
DISO_to_ANAT16img Bone structure of sacrum C0036037
DISO_to_DISO14img COMPL POSTOP C0032787
DISO_to_DISO14img Cerebrospinal Fluid Rhinorrhea C0007815
DISO_to_DISO13img Abnormalities, Multiple C0000772
DISO_to_DISO10img Neurofibromatosis 1 C0027831
DISO_to_ANAT8img Ethmoid Bone C0015027
DISO_to_DISO8img COMPL POSTOP C0032787
DISO_to_ANAT7img Bone structure of lumbar vertebra C0024091
DISO_to_DISO7img Abnormalities, Multiple C0000772
DISO_to_DISO7img CSF - Cerebrospinal rhinorrhea C0007815
DISO_to_DISO7img Cyst C0010709
DISO_to_DISO7img Spinal Cord Diseases C0037928
DISO_to_ANAT6img Base of skull structure C0149543
DISO_to_ANAT6img Bone structure of thoracic vertebra C0039987
DISO_to_ANAT6img Cervical Vertebrae C0728985
DISO_to_ANAT6img Dura Mater C0013313
DISO_to_ANAT6img Sphenoid Sinus C0037885
DISO_to_DISO6img Compression of spinal cord C0037926
DISO_to_DISO6img Meningitis C0025289
DISO_to_DISO6img Neural Tube Defects C0027794
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanSC5DL6309
img OMIM, Score=833, UMLKSK CUI: C0025299
HumanMNX13110motor neuron and pancreas homeobox 1
img OMIM, Score=833, UMLKSK CUI: C0025299
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0025299Meningocele0self