Human Phenotype Ontology

Last uploaded: April 15, 2019
Preferred Name

Hydrops fetalis

Definitions

The most common causes of hydrops fetalis are hematologic (inclusing isoimmunization because of Rhesus incompatibility and other causes), hereditary hemolytic disorders, fetal hemorrhage, disorders of red cell production), cardiovascular disorders, infections, certain intrathoracic malformations, and idiopathic forms. The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema.

ID

http://purl.obolibrary.org/obo/HP_0001789

comment

The most common causes of hydrops fetalis are hematologic (inclusing isoimmunization because of Rhesus incompatibility and other causes), hereditary hemolytic disorders, fetal hemorrhage, disorders of red cell production), cardiovascular disorders, infections, certain intrathoracic malformations, and idiopathic forms.

database_cross_reference

SNOMEDCT_US:276508000

UMLS:C0020305

MSH:D015160

definition

The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema.

has_obo_namespace

human_phenotype

id

HP:0001789

label

Hydrops fetalis

notation

HP:0001789

prefLabel

Hydrops fetalis

treeView

http://purl.obolibrary.org/obo/HP_0000969

http://purl.obolibrary.org/obo/HP_0001197

subClassOf

http://purl.obolibrary.org/obo/HP_0000969

http://purl.obolibrary.org/obo/HP_0001197

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http://phenomebrowser.net/ontologies/mesh/mesh.owl#D015160 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C23.888.277.395 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.378.420.826.100.350 RH-MESH LOOM
http://purl.bioontology.org/ontology/MEDDRA/10020526 MEDDRA LOOM
http://purl.obolibrary.org/obo/HP_0001789 HOOM SAME_URI
http://purl.obolibrary.org/obo/HP_0001789 UPHENO LOOM
http://purl.obolibrary.org/obo/HP_0001789 UPHENO SAME_URI
http://purl.obolibrary.org/obo/HP_0001789 NIFSTD LOOM
http://purl.obolibrary.org/obo/HP_0001789 NIFSTD SAME_URI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84767 NCIT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84767 NCIT LOOM
http://purl.obolibrary.org/obo/MP_0002192 MP LOOM
http://purl.obolibrary.org/obo/MP_0002192 MP LOOM
http://purl.obolibrary.org/obo/MP_0002192 MP LOOM
http://purl.obolibrary.org/obo/MP_0002192 UPHENO LOOM
http://purl.obolibrary.org/obo/MP_0002192 MP LOOM
http://www.pepathway.org/peo/1.2#Hydrops_fetalis PE-O LOOM
http://www.limics.org/hrdo/rdfns#pat_id_1347 HRDO LOOM
http://purl.bioontology.org/ontology/RCD/Xa07a RCD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.378.120.413.480 RH-MESH LOOM
http://purl.jp/bio/4/id/200906093810722040 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C20.188.413.480 RH-MESH LOOM
http://purl.obolibrary.org/obo/DOID_1097 DOID LOOM
http://purl.bioontology.org/ontology/MESH/D015160 MESH LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2605 IFAR LOOM
http://purl.bioontology.org/ontology/WHO/1129 WHO-ART LOOM
http://www.limics.org/hrdo/rdfns#sgn_id_55160 HRDO LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU009460 OMIM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.300.060.480 RH-MESH LOOM
http://www.orpha.net/ORDO/Orphanet_1041 ORDO LOOM
http://www.orpha.net/ORDO/Orphanet_1041 HORD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C13.703.277.060.480 RH-MESH LOOM
http://purl.org/obo/owl/HP#HP_0001789 BDO LOOM
http://radlex.org/RID/RID39322 RADLEX LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hydrops_Fetalis CSEO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.365.826.100.350 RH-MESH LOOM
http://scdontology.h3abionet.org/ontology/SCDO_0000578 SCDO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/276508000 SNOMEDCT LOOM