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Details
Link-It Detail - Disease - Primary Dysautonomias
Debug Stats
  • ### Total Build Time: 101 ms 15.989 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 471 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=15 ms Completed: 15 ms rowSize= 569 bytes
  • CONCEPT_CHILDREN gt=13 ms Completed: 13 ms rowSize= 1.839 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 1.536 KB
  • CONCEPT_RELATIONSHIPS gt=34 ms Completed: 34 ms rowSize= 6.216 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 3.685 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Disease (1)
Primary Dysautonomias C0013363
Definition (1)
An acute or chronic disorder, affecting the sympathetic or parasympathetic nervous system. It can be primary, the result of central nervous system degeneration, or secondary due to diabetes or alcoholism. Patients with the chronic form of this disorder usually have a progressive clinical course and a poor prognosis.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Autonomic Nervous System Diseases C1145628
Children (4)
img Multiple System Atrophy C0393571
img Orthostatic Intolerance C1535893
img Pure Autonomic Failure C0393911
img Dysautonomia, Familial C0013364
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Autonomic Nervous System Diseases C11456283img Autonomic Nervous System Diseases C1145628
Relationships (12)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 8


Relationships:
none : 6
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
mapped_​to : 3
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_DISO14img Parkinson Disease C0030567
DISO_to_CHEM9img Abs - Autoantibodies C0004358
DISO_to_DISO8img AUTOIMMUNE DIS NERVOUS SYSTEM C0751871
DISO_to_ANAT7img Autonomic ganglion C0017068
DISO_to_DISO7img Brain Injuries C0270611
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Peripheral Nerves C0031119
DISO_to_DISOmapped_toimg AUTONOMIC INSTABILITY C0262385
DISO_to_DISOmapped_toimg Acute cholinergic dysautonomia C2930973
DISO_to_DISOpermuted_term_ofimg Dysautonomia C0013363
DISO_to_DISOmapped_toimg Dysautonomia like disorder C1857153
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanPRNP5621prion protein
img OMIM, Score=1000, UMLKSK CUI: C0013363
HumanLIFR3977leukemia inhibitory factor receptor alpha
img OMIM, Score=1000, UMLKSK CUI: C0013363
img OMIM, Score=1000, UMLKSK CUI: C0013363
HumanLEP3952leptin
img GENERIF, Score=861, Pubmed Id: 18226448, UMLKSK CUI: C0013363
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0013363Primary Dysautonomias0self