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Details
Link-It Detail - Disease - Polyhydramnios
Debug Stats
  • ### Total Build Time: 111 ms 38.574 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 457 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=10 ms Completed: 10 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.547 KB
  • CONCEPT_RELATIONSHIPS gt=45 ms Completed: 45 ms rowSize= 10.285 KB
  • CONCEPT_GENES gt=40 ms Completed: 40 ms rowSize= 24.064 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Polyhydramnios C0020224
Definition (1)
A condition of abnormally high AMNIOTIC FLUID volume, such as greater than 2,000 ml in the LAST TRIMESTER and usually diagnosed by ultrasonographic criteria (AMNIOTIC FLUID INDEX). It is associated with maternal DIABETES MELLITUS; MULTIPLE PREGNANCY; CHROMOSOMAL DISORDERS; and congenital abnormalities.
Semantic Types (1)
Pathologic Function (T046)
Parents (1)
img Pregnancy Complications C0032962
Ancestral Roots
RootRoot Plus OneDepthParent
img Female Urogenital Diseases and Pregnancy Complications C1720765img Pregnancy Complications C00329623img Pregnancy Complications C0032962
Relationships (24)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 1
diso_​to_​diso : 17
diso_​to_​phen : 1


Relationships:
none : 19
associated_​with : 1
isa : 2
location_​of : 1
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN12img genetic aspects C0017399
DISO_to_ANAT10img Amniotic Fluid C0002638
DISO_to_ANAT8img Amniotic Fluid C0002638
DISO_to_DISO8img Fetofetal Transfusion C0015958
DISO_to_DISO7img Complication Aspects C1171258
DISO_to_DISO7img Oligohydramnios C0079924
DISO_to_DISO6img Abnormalities, Multiple C0000772
DISO_to_DISO6img DISORDER FETAL C0015929
DISO_to_DISO5img Oligohydramnios C0079924
DISO_to_ANAT4img Fetus C0015965
DISO_to_ANAT3img Placenta C0032043
DISO_to_CHEM3img Indomethacin C0021246
DISO_to_DISO3img Abnormalities, Multiple C0000772
DISO_to_DISO3img Bartter Disease C0004775
DISO_to_DISO3img Congenital Heart Defects C0018798
DISO_to_DISO3img Fetofetal Transfusion C0015958
DISO_to_DISO3img OUTCOME PREGN C0032972
DISO_to_DISO3img Placenta Diseases C0032045
DISO_to_DISO3img Pregnancy Complications C0032962
DISO_to_ANATlocation_ofimg Amniotic Fluid C0002638
DISO_to_DISOmapped_toimg Arthrosis, flat face, hypotonia, short neck and macrocephaly C1855605
DISO_to_DISOassociated_withimg Increased amniotic fluid production C0686774
DISO_to_DISOisaimg Polyhydramnios - delivered C0405046
DISO_to_DISOisaimg Polyhydramnios with antenatal problem C0405045
Genes (38)

Species:
human : 38
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHYLS1219844hydrolethalus syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanEBP10682emopamil binding protein (sterol isomerase)
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanZMPSTE2410269zinc metallopeptidase STE24
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanCD9610225CD96 molecule
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanYWHAE7531tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanSOX96662SRY (sex determining region Y)-box 9
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanRAPSN5913receptor-associated protein of the synapse
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanPTH1R5745parathyroid hormone 1 receptor
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanMAP2K25605mitogen-activated protein kinase kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanPAFAH1B15048platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanNPPB4879natriuretic peptide B
img GENERIF, Score=1000, Pubmed Id: 12861161, UMLKSK CUI: C0020224
HumanNPPA4878natriuretic peptide A
img GENERIF, Score=1000, Pubmed Id: 16113566, UMLKSK CUI: C0020224
HumanNEB4703nebulin
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanMYCN4613v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanMTM14534myotubularin 1
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanLMNA4000lamin A/C
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanKRAS3845Kirsten rat sarcoma viral oncogene homolog
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanHSD17B43295hydroxysteroid (17-beta) dehydrogenase 4
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanHRAS3265Harvey rat sarcoma viral oncogene homolog
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanGBE12632glucan (1,4-alpha-), branching enzyme 1
img OMIM, Score=1000, UMLKSK CUI: C0020224
HumanGBA2629glucosidase, beta, acid
img OMIM, Score=1000, UMLKSK CUI: C0020224
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020224Polyhydramnios0self