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 - AUTONOMIC NEUROPATHY
Debug Stats
  • ### Total Build Time: 36 ms 19.090 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 467 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=15 ms Completed: 15 ms rowSize= 7.722 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 9.357 KB
  • CONCEPT_XREFS gt=10 ms Completed: 10 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
AUTONOMIC NEUROPATHY C0259749
Definition (1)
An inherited or acquired peripheral neuropathy affecting the autonomic nervous system. It results in disruption of the involuntary body functions. Inherited causes include Fabry disease and porphyrias. Acquired causes include diabetes, uremia, hepatic disorders, vitamin deficiencies, toxins, and drug toxicities.
Relationships (16)

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


Relationships:
clinically_​similar : 9
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 3
used_​for : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATused_forimg Autonomic Nervous System C0004388
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Peripheral Nerves C0031119
DISO_to_DISOclinically_similarimg AMYLOID NEUROPATHY SECOND C0751660
DISO_to_DISOclinically_similarimg AUTONOMIC NEUROPATHY C0259749
DISO_to_DISOclinically_similarimg Aut neuropthy in oth dis C0154691
DISO_to_DISOisaimg Autonomic Neuropathies, Diabetic C0271686
DISO_to_DISOclinically_similarimg Autosomal recessive sensory neuropathy C0270914
DISO_to_DISOisaimg Diabetic autonomic neuropathy associated with type 1 diabetes mellitus C1960678
DISO_to_DISOisaimg Diabetic autonomic neuropathy associated with type 2 diabetes mellitus C1827612
DISO_to_DISOclinically_similarimg Dysautonomia, Familial C0013364
DISO_to_DISOclinically_similarimg HSAN Type IV C0020074
DISO_to_DISOclinically_similarimg Hereditary Sensory Autonomic Neuropathy, Type 1 C0020071
DISO_to_DISOclinically_similarimg Hereditary Sensory Autonomic Neuropathy, Type 5 C0020075
DISO_to_DISOclinically_similarimg Idiopathic peripheral autonomic neuropathy C0154690
DISO_to_DISOused_forimg Nervous System Diseases C0027765
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanWNK165125WNK lysine deficient protein kinase 1
img GENERIF, Score=1000, Pubmed Id: 15060842, UMLKSK CUI: C0259749
HumanSPTLC110558serine palmitoyltransferase, long chain base subunit 1
img GENERIF, Score=673, Pubmed Id: 18018475, UMLKSK CUI: C0259749
HumanRAB7A7879RAB7A, member RAS oncogene family
img OMIM, Score=666, UMLKSK CUI: C0259749
HumanPPY5539pancreatic polypeptide
img GENERIF, Score=1000, Pubmed Id: 12187924, UMLKSK CUI: C0259749
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
img GENERIF, Score=694, Pubmed Id: 12102460, UMLKSK CUI: C0259749
img GENERIF, Score=694, Pubmed Id: 12210794, UMLKSK CUI: C0259749
HumanNPY4852neuropeptide Y
img GENERIF, Score=1000, Pubmed Id: 12187924, UMLKSK CUI: C0259749
HumanNGF4803nerve growth factor (beta polypeptide)
img GENERIF, Score=694, Pubmed Id: 18420729, UMLKSK CUI: C0259749
HumanHMBS3145hydroxymethylbilane synthase
img OMIM, Score=1000, UMLKSK CUI: C0259749
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0259749AUTONOMIC NEUROPATHY0self