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Details
Link-It Detail - Disease - Hydrops Fetalis
Debug Stats
  • ### Total Build Time: 129 ms 45.940 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 422 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 1.385 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=48 ms Completed: 48 ms rowSize= 11.908 KB
  • CONCEPT_RELATIONSHIPS gt=41 ms Completed: 41 ms rowSize= 12.411 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 18.140 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hydrops Fetalis C0020305
Definition (1)
Abnormal accumulation of serous fluid in two or more fetal compartments, such as SKIN; PLEURA; PERICARDIUM; PLACENTA; PERITONEUM; AMNIOTIC FLUID. General fetal EDEMA may be of non-immunologic origin, or of immunologic origin as in the case of ERYTHROBLASTOSIS FETALIS.
Semantic Types (1)
Sign or Symptom (T184)
Parents (3)
img Erythroblastosis, Fetal C0014761
img Edema C0013604
img alpha-Thalassemia C0002312
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Erythroblastosis, Fetal C0014761
img Immune System Diseases C0021053img Blood Group Incompatibility C00058064img Erythroblastosis, Fetal C0014761
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Infant, Newborn, Diseases C00212904img Erythroblastosis, Fetal C0014761
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Fetal Diseases C00159294img Erythroblastosis, Fetal C0014761
img Female Urogenital Diseases and Pregnancy Complications C1720765img Pregnancy Complications C00329625img Erythroblastosis, Fetal C0014761
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370884img Edema C0013604
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189396img alpha-Thalassemia C0002312
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501236img alpha-Thalassemia C0002312
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189398img alpha-Thalassemia C0002312
Relationships (32)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 2
diso_​to_​diso : 25
diso_​to_​phen : 2


Relationships:
none : 27
isa : 2
mapped_​to : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN46img genetic aspects C0017399
DISO_to_PHEN26img genetic aspects C0017399
DISO_to_DISO22img DISORDER FETAL C0015929
DISO_to_DISO20img Complication Aspects C1171258
DISO_to_CHEM19img Abnormal Hemoglobins C0019047
DISO_to_DISO19img COMPL PREGN INFECT C0032965
DISO_to_DISO17img alpha-Thalassemia C0002312
DISO_to_DISO16img Disease due to Parvoviridae C0276275
DISO_to_DISO15img Disease due to Parvoviridae C0276275
DISO_to_ANAT13img Fetus C0015965
DISO_to_DISO13img DISORDER FETAL C0015929
DISO_to_ANAT12img Placenta C0032043
DISO_to_DISO12img COMPL PREGN INFECT C0032965
DISO_to_ANAT11img In Blood C0005768
DISO_to_DISO11img Pregnancy Complications C0032962
DISO_to_DISO10img Teratoma C0039538
DISO_to_DISO9img Congenital Heart Defects C0018798
DISO_to_DISO9img Fetal Death C0015927
DISO_to_DISO9img Pre-Eclampsia C0032914
DISO_to_DISO9img Pregnancy Complications C0032962
DISO_to_DISO9img alpha-Thalassemia C0002312
DISO_to_DISO8img Abnormalities, Multiple C0000772
DISO_to_DISO8img Placenta Diseases C0032045
DISO_to_DISO8img Rh Isoimmunization C0035404
DISO_to_CHEM7img Abnormal Hemoglobins C0019047
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanCDAN1146059codanin 1
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanALG156052ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanTALDO16888transaldolase 1
img GENERIF, Score=1000, Pubmed Id: 17095351, UMLKSK CUI: C0020305
HumanPTH1R5745parathyroid hormone 1 receptor
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanPKLR5313pyruvate kinase, liver and RBC
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanNEU14758sialidase 1 (lysosomal sialidase)
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanHADHB3032hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanHADHA3030hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanGUSB2990glucuronidase, beta
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanGLE12733GLE1 RNA export mediator
img OMIM, Score=882, UMLKSK CUI: C0020305
HumanGBE12632glucan (1,4-alpha-), branching enzyme 1
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanGBA2629glucosidase, beta, acid
img OMIM, Score=1000, UMLKSK CUI: C0020305
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanFLT42324fms-related tyrosine kinase 4
img OMIM, Score=833, UMLKSK CUI: C0020305
HumanERBB32065v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 3
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanSLC26A21836solute carrier family 26 (anion exchanger), member 2
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanCOL2A11280collagen, type II, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
img OMIM, Score=1000, UMLKSK CUI: C0020305
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
img OMIM, Score=1000, UMLKSK CUI: C0020305
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020305Hydrops Fetalis0self