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Details
Link-It Detail - Disease - Meningomyelocele
Debug Stats
  • ### Total Build Time: 77 ms 23.742 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 249 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=5 ms Completed: 5 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.836 KB
  • CONCEPT_RELATIONSHIPS gt=61 ms Completed: 61 ms rowSize= 13.351 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 5.076 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Meningomyelocele C0025312
Definition (1)
hernial protrusion of the spinal cord and its meninges through a defect in the vertebral canal.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Neural Tube Defects C0027794
Ancestral Roots
RootRoot Plus OneDepthParent
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 (61)

Relation Types:
diso_​to_​anat : 12
diso_​to_​diso : 46
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 37
associated_​with : 2
is_​associated_​anatomic_​site_​of : 2
isa : 10
location_​of : 3
mapped_​to : 4
permuted_​term_​of : 1
use : 2
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO153img Complication Aspects C1171258
DISO_to_DISO134img Complication Aspects C1171258
DISO_to_DISO50img Spina Bifida C0080178
DISO_to_DISO27img DISORDER FETAL C0015929
DISO_to_DISO24img Spina Bifida C0080178
DISO_to_DISO23img DISORDER FETAL C0015929
DISO_to_DISO23img Neurogenic Urinary Bladder C0005697
DISO_to_ANAT21img Spinal Cord C0037925
DISO_to_ANAT20img Fetus C0015965
DISO_to_DISO20img Hydrocephalus C0020255
DISO_to_DISO20img Neural Tube Defects C0027794
DISO_to_DISO19img Abnormalities, Multiple C0000772
DISO_to_DISO19img Hydrocephalus C0020255
DISO_to_DISO18img Neurogenic Urinary Bladder C0005697
DISO_to_ANAT17img Surgical Flaps C0038925
DISO_to_DISO17img Arnold Chiari Malformation C0003803
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_ANAT16img Fetus C0015965
DISO_to_DISO14img COMPL POSTOP C0032787
DISO_to_ANAT12img Spinal Cord C0037925
DISO_to_ANAT12img Surgical Flaps C0038925
DISO_to_DISO12img Gait C0016928
DISO_to_DISO11img Lipoma C0023798
DISO_to_DISO11img Scoliosis C0036439
DISO_to_DISO10img Fecal Incontinence C0015732
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img OMIM, Score=1000, UMLKSK CUI: C0025312
HumanFRAS180144Fraser syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0025312
HumanPORCN64840porcupine homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0025312
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
img GENERIF, Score=861, Pubmed Id: 16237707, UMLKSK CUI: C0025312
HumanLEP3952leptin
img GENERIF, Score=1000, Pubmed Id: 12218376, UMLKSK CUI: C0025312
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0025312Meningomyelocele0self