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Details
Link-It Detail - Human Phenotype - Abnormal autonomic nervous system morphology
Debug Stats
  • ### Total Build Time: 31 ms 16.521 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 464 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 457 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.179 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 12.827 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.038 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Human Phenotype (1)
Abnormal autonomic nervous system morphology HP:0012331
Definition (1)
A structural abnormality of the `autonomic nervous system` (FMA:9905).
Parents (1)
img Abnormality of the autonomic nervous system HP:0002270
Children (1)
img Abnormality of the enteric ganglia HP:0004362
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the autonomic nervous system HP:0002270
Genes (55)

Species:
human : 55
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanTRIP4Q32.1Q32.2100529228
HumanHSCR5404720Hirschsprung disease, susceptibility to, 5
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
HumanSALL457167sal-like 4 (Drosophila)
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
HumanBBS927241Bardet-Biedl syndrome 9
HumanKIAA127926128KIAA1279
HumanTRIM3222954tripartite motif containing 32
HumanSDCCAG810806serologically defined colon cancer antigen 8
HumanSF3B410262splicing factor 3b, subunit 4, 49kDa
HumanZEB29839zinc finger E-box binding homeobox 2
HumanPHOX2B8929paired-like homeobox 2b
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012331Abnormal autonomic nervous system morphology0self