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 - Pseudobulbar Palsy
Debug Stats
  • ### Total Build Time: 127 ms 20.930 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 602 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=2 ms Completed: 2 ms rowSize= 232 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 545 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.788 KB
  • CONCEPT_RELATIONSHIPS gt=75 ms Completed: 75 ms rowSize= 7.995 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 7.286 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Pseudobulbar Palsy C0033790
Definition (1)
A syndrome characterized by DYSARTHRIA, dysphagia, dysphonia, impairment of voluntary movements of tongue and facial muscles, and emotional lability. This condition is caused by diseases that affect the motor fibers that travel from the cerebral cortex to the lower BRAIN STEM (i.e., corticobulbar tracts); including MULTIPLE SCLEROSIS; MOTOR NEURON DISEASE; and CEREBROVASCULAR DISORDERS. (From Adams et al., Principles of Neurology, 6th ed, p489)
Semantic Types (2)
Disease or Syndrome (T047)
Finding (T033)
Parents (1)
img Paralysis C0522224
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Paralysis C0522224
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Paralysis C0522224
Relationships (17)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 3
diso_​to_​diso : 13


Relationships:
none : 10
classifies : 2
isa : 1
mapped_​to : 2
permuted_​term_​of : 1
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO6img Complication Aspects C1171258
DISO_to_DISO5img Mood Disorders C0525045
DISO_to_CHEM4img Dextromethorphan C0011816
DISO_to_DISO4img Amyotrophic Lateral Sclerosis C0002736
DISO_to_ANAT3img Brain C0006104
DISO_to_CHEM3img Dextromethorphan C0011816
DISO_to_CHEM3img Quinidine C0034414
DISO_to_DISO3img Complication Aspects C1171258
DISO_to_DISO3img Deglutition Disorders C0011168
DISO_to_DISO3img Motor Neuron Disease C0085084
DISO_to_DISOpermuted_term_ofimg Bulbar Palsies, Spastic C0033790
DISO_to_DISOmapped_toimg Congenital pseudobulbar palsy C0394009
DISO_to_DISOmapped_toimg Kuzniecky Andermann syndrome C2931598
DISO_to_DISOclassifiesimg Other and unspecified hereditary and degenerative nervous conditions C0810267
DISO_to_DISOclassifiesimg Other hereditary and degenerative nervous system conditions C0809991
DISO_to_DISOisaimg Progressive pseudobulbar palsy C0393549
DISO_to_DISOused_forimg Progressive supranuclear palsy C0038868
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanSOD16647superoxide dismutase 1, soluble
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanPRPH5630peripherin
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanNOTCH34854notch 3
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanNEFH4744neurofilament, heavy polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanLMNB14001lamin B1
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanDCTN11639dynactin 1
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanCYP27A11593cytochrome P450, family 27, subfamily A, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0033790
HumanANG283angiogenin, ribonuclease, RNase A family, 5
img OMIM, Score=1000, UMLKSK CUI: C0033790
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0033790Pseudobulbar Palsy0self