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Details
Link-It Detail - Human Phenotype - Abnormality of the autonomic nervous system
Debug Stats
  • ### Total Build Time: 23 ms 22.146 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 218 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 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
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  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 454 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.995 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.169 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 15.935 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.037 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the autonomic nervous system HP:0002270
Definition (1)
An abnormality of the `autonomic nervous system` (FMA:9905).
Parents (1)
img Abnormality of the nervous system HP:0000707
Children (9)
img Hypothermia HP:0002045
img Abnormal autonomic nervous system physiology HP:0012332
img Horner syndrome HP:0002277
img Orthostatic hypotension HP:0001278
img Dysautonomia HP:0002459
img Autonomic dysregulation HP:0002271
img Autonomic dysfunction HP:0002387
img Orthostatic tachycardia HP:0012173
img Abnormal autonomic nervous system morphology HP:0012331
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the nervous system HP:0000707
Genes (108)

Species:
human : 108
Page Size
Current 25
  Page 1 of 5
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanTRIP4Q32.1Q32.2100529228
HumanMGS100126595Mungen syndrome
img HP TAS, OMIM ID: 611376
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanHSCR5404720Hirschsprung disease, susceptibility to, 5
HumanBRAT1221927BRCA1-associated ATM activator 1
img HP RolledUp, OMIM ID: 614498
HumanPARK10170534Parkinson disease 10 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanARX170302aristaless related homeobox
HumanBBS12166379Bardet-Biedl syndrome 12
HumanBBS5129880Bardet-Biedl syndrome 5
HumanB3GALT6126792UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
HumanTTC8123016tetratricopeptide repeat domain 8
HumanTMEM6791147transmembrane protein 67
HumanARL684100ADP-ribosylation factor-like 6
HumanCEP29080184centrosomal protein 290kDa
HumanBBS1079738Bardet-Biedl syndrome 10
HumanCCDC28B79140coiled-coil domain containing 28B
HumanPARK460454Parkinson disease (autosomal dominant, Lewy body) 4
img HP RolledUp, OMIM ID: 605543
HumanSALL457167sal-like 4 (Drosophila)
HumanC10orf256652chromosome 10 open reading frame 2
img HP RolledUp, OMIM ID: 251880
HumanPIGV55650phosphatidylinositol glycan anchor biosynthesis, class V
HumanBBS755212Bardet-Biedl syndrome 7
HumanMKS154903Meckel syndrome, type 1
HumanMBTPS251360membrane-bound transcription factor peptidase, site 2
HumanWDPCP51057WD repeat containing planar cell polarity effector
HumanOHDS50948Orthostatic hypotensive disorder of Streeten
img HP RolledUp, OMIM ID: 143850
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002270Abnormality of the autonomic nervous system0self