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Details
Link-It Detail - Disease - 213 CONGENITAL HYPOPLASIAS
Debug Stats
  • ### Total Build Time: 215 ms 16.206 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 350 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=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=188 ms Completed: 188 ms rowSize= 13.075 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 1.559 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
213 CONGENITAL HYPOPLASIAS C0020636
Relationships (128)

Relation Types:
diso_​to_​diso : 128


Relationships:
associated_​with : 125
isa : 3
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOassociated_withimg AI - Amelogenesis imperfecta C0002452
DISO_to_DISOassociated_withimg ASPLENIA, FAMILIAL C0685889
DISO_to_DISOassociated_withimg Achondrogenesis C0001079
DISO_to_DISOassociated_withimg Ageneses, Enamel C0011351
DISO_to_DISOassociated_withimg Amyotrophia congenita C0265520
DISO_to_DISOassociated_withimg Ascending aortic hypoplasia C0265882
DISO_to_DISOassociated_withimg Atelomyelia C0266511
DISO_to_DISOassociated_withimg CEREBELLAR HYPOPLASIA C0266470
DISO_to_DISOassociated_withimg CLAVICULAR HYPOPLASIA C0426799
DISO_to_DISOassociated_withimg Cleidocranial Dysplasia C0008928
DISO_to_DISOisaimg Congenital decrease in cellularity C0332913
DISO_to_DISOassociated_withimg Congenital fleshy tail tab C0685610
DISO_to_DISOassociated_withimg Congenital hyperplasia of intrahepatic bile duct C0266243
DISO_to_DISOassociated_withimg Congenital hypoplasia of adrenal gland C0220766
DISO_to_DISOassociated_withimg Congenital hypoplasia of alisphenoid bone C0685264
DISO_to_DISOassociated_withimg Congenital hypoplasia of aorta C0265892
DISO_to_DISOassociated_withimg Congenital hypoplasia of aortic arch C0265881
DISO_to_DISOassociated_withimg Congenital hypoplasia of aortic valve C0542515
DISO_to_DISOassociated_withimg Congenital hypoplasia of arch of caudal vertebra C0685594
DISO_to_DISOassociated_withimg Congenital hypoplasia of arch of cervical vertebra C0685488
DISO_to_DISOassociated_withimg Congenital hypoplasia of arch of lumbar vertebra C0685538
DISO_to_DISOassociated_withimg Congenital hypoplasia of arch of sacral vertebra C0685566
DISO_to_DISOassociated_withimg Congenital hypoplasia of arch of thoracic vertebra C0685513
DISO_to_DISOassociated_withimg Congenital hypoplasia of basioccipital bone C0685288
DISO_to_DISOassociated_withimg Congenital hypoplasia of basisphenoid bone C0685272
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanHESX18820HESX homeobox 1
img GAD, Score=819, Pubmed Id: 11136712, UMLKSK CUI: C0020636
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020636213 CONGENITAL HYPOPLASIAS0self