Human Phenotype Ontology

Last uploaded: October 9, 2018
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 Robert Hoehndorf Version of MeSH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C23.888.277.395 Robert Hoehndorf Version of MeSH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.378.420.826.100.350 Robert Hoehndorf Version of MeSH LOOM
http://purl.bioontology.org/ontology/MEDDRA/10020526 Medical Dictionary for Regulatory Activities LOOM
http://purl.obolibrary.org/obo/HP_0001789 Children's Health Exposure Analysis Resource LOOM
http://purl.obolibrary.org/obo/HP_0001789 Children's Health Exposure Analysis Resource SAME_URI
http://purl.obolibrary.org/obo/HP_0001789 HPO - ORDO Ontological Module SAME_URI
http://purl.obolibrary.org/obo/HP_0001789 Combined Phenotype Ontology LOOM
http://purl.obolibrary.org/obo/HP_0001789 Combined Phenotype Ontology SAME_URI
http://purl.obolibrary.org/obo/HP_0001789 Neuroscience Information Framework (NIF) Standard Ontology LOOM
http://purl.obolibrary.org/obo/HP_0001789 Neuroscience Information Framework (NIF) Standard Ontology SAME_URI
http://purl.obolibrary.org/obo/HP_0001789 Monarch Disease Ontology LOOM
http://purl.obolibrary.org/obo/HP_0001789 Monarch Disease Ontology SAME_URI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84767 National Cancer Institute Thesaurus LOOM
http://purl.obolibrary.org/obo/MP_0002192 Mammalian Phenotype Ontology LOOM
http://purl.obolibrary.org/obo/MP_0002192 Combined Phenotype Ontology LOOM
http://www.pepathway.org/peo/1.2#Hydrops_fetalis Pre-eclampsia Ontology LOOM
http://www.limics.org/hrdo/rdfns#pat_id_1347 Disease core ontology applied to Rare Diseases LOOM
http://purl.bioontology.org/ontology/RCD/Xa07a Read Codes, Clinical Terms Version 3 (CTV3) LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.378.120.413.480 Robert Hoehndorf Version of MeSH LOOM
http://purl.jp/bio/4/id/200906093810722040 Interlinking Ontology for Biological Concepts LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C20.188.413.480 Robert Hoehndorf Version of MeSH LOOM
http://purl.obolibrary.org/obo/DOID_1097 Human Disease Ontology LOOM
http://purl.obolibrary.org/obo/DOID_1097 Neuroscience Information Framework (NIF) Standard Ontology LOOM
http://purl.bioontology.org/ontology/MESH/D015160 Medical Subject Headings LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2605 Fanconi Anemia Ontology LOOM
http://purl.bioontology.org/ontology/WHO/1129 World Health Organization (WHO) Adverse Reaction Terminology LOOM
http://www.limics.org/hrdo/rdfns#sgn_id_55160 Disease core ontology applied to Rare Diseases LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU009460 Online Mendelian Inheritance in Man LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.300.060.480 Robert Hoehndorf Version of MeSH LOOM
http://www.radlex.org/RID/#RID39322 Radiology Lexicon LOOM
http://www.orpha.net/ORDO/Orphanet_1041 Orphanet Rare Disease Ontology LOOM
http://www.orpha.net/ORDO/Orphanet_1041 Holistic Ontology of Rare Diseases LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C13.703.277.060.480 Robert Hoehndorf Version of MeSH LOOM
http://www.gamuts.net/entity#hydrops_fetalis Radiology Gamuts Ontology LOOM
http://purl.org/obo/owl/HP#HP_0001789 Bone Dysplasia Ontology LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hydrops_Fetalis Cigarette Smoke Exposure Ontology LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.365.826.100.350 Robert Hoehndorf Version of MeSH LOOM
http://scdontology.h3abionet.org/ontology/SCDO_0000578 Sickle Cell Disease Ontology LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/276508000 SNOMED CT LOOM