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Details
Link-It Detail - Human Phenotype - Abnormal autonomic nervous system physiology
Debug Stats
  • ### Total Build Time: 100 ms 27.460 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 219 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 224 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 464 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 2.017 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.179 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=54 ms Completed: 54 ms rowSize= 22.196 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal autonomic nervous system physiology HP:0012332
Definition (1)
A functional abnormality of the `autonomic nervous system` (FMA:9905).
Parents (1)
img Abnormality of the autonomic nervous system HP:0002270
Children (6)
img Abnormal sudomotor regulation HP:0012333
img Horner syndrome HP:0002277
img Orthostatic hypotension HP:0001278
img Dysautonomia HP:0002459
img Autonomic dysregulation HP:0002271
img Orthostatic tachycardia HP:0012173
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the autonomic nervous system HP:0002270
Genes (43)

Species:
human : 43
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanBRAT1221927BRCA1-associated ATM activator 1
img HP RolledUp, OMIM ID: 614498
HumanPARK10170534Parkinson disease 10 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanPARK460454Parkinson disease (autosomal dominant, Lewy body) 4
img HP RolledUp, OMIM ID: 605543
HumanOHDS50948Orthostatic hypotensive disorder of Streeten
img HP RolledUp, OMIM ID: 143850
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
img HP RolledUp, OMIM ID: 146500
HumanFGF2026281fibroblast growth factor 20
img HP RolledUp, OMIM ID: 168600
HumanKIF1B23095kinesin family member 1B
img HP RolledUp, OMIM ID: 256700
HumanWDR4511152WD repeat domain 45
img HP RolledUp, OMIM ID: 300894
HumanSNCAIP9627synuclein, alpha interacting protein
img HP RolledUp, OMIM ID: 168600
HumanOSMR9180oncostatin M receptor
HumanPHOX2B8929paired-like homeobox 2b
img HP RolledUp, OMIM ID: 256700
HumanIKBKAP8518inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
img HP RolledUp, OMIM ID: 223900
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
img HP RolledUp, OMIM ID: 231550
HumanUCHL17345ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
img HP RolledUp, OMIM ID: 168600
HumanTTR7276transthyretin
img HP RolledUp, OMIM ID: 105210
HumanTBP6908TATA box binding protein
img HP RolledUp, OMIM ID: 168600
HumanSOX106663SRY (sex determining region Y)-box 10
img HP RolledUp, OMIM ID: 277580
img HP RolledUp, OMIM ID: 609136
HumanSNCA6622synuclein, alpha (non A4 component of amyloid precursor)
img HP RolledUp, OMIM ID: 605543
HumanSLC6A26530solute carrier family 6 (neurotransmitter transporter), member 2
img HP RolledUp, OMIM ID: 604715
HumanPRNP5621prion protein
img HP RolledUp, OMIM ID: 600072
HumanPARK35072Parkinson disease 3 (autosomal dominant, Lewy body)
img HP RolledUp, OMIM ID: 168600
HumanNR4A24929nuclear receptor subfamily 4, group A, member 2
img HP RolledUp, OMIM ID: 168600
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
img HP RolledUp, OMIM ID: 256800
HumanNME14830NME/NM23 nucleoside diphosphate kinase 1
img HP RolledUp, OMIM ID: 256700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012332Abnormal autonomic nervous system physiology0self