hydrops fetalis
Hydrops fetalis is a severe and challenging fetal condition usually defined as the excessive accumulation of fetal fluid within the fetal extravascular compartments and body cavities that manifests as edema, pleural and pericardial effusion and ascites. It is the end-stage of a wide variety of disorders. The cause may be immunologic (immune hydrops fetalis, IHF) or non immunologic (non-immune hydrops fetalis, NIHF), depending on the presence or absence of maternal antibodies against fetal red cell antigens (ABO incompatibility or rhesus (Rh) incompatibility). [ Orphanet:1041 ]
Term info
- HP:0001789 (MONDO:otherHierarchy)
- SCTID:276508000 (MONDO:equivalentTo)
- NCIT:C84767 (MONDO:equivalentTo)
- MedDRA:10020529 (Orphanet:1041/e)
- UMLS:C0020305 (Orphanet:1041/e)
- GARD:0002301 (MONDO:equivalentTo)
- GARD:0002783 (MONDO:equivalentTo)
- Orphanet:1041 (MONDO:equivalentTo)
- MESH:D015160 (https://orcid.org/0000-0003-1967-3726)
gard_rare, ordo_malformation_syndrome
hydrops fetalis (disease)
http://identifiers.org/meddra/10020529
Hydrops fetalis is a severe and challenging fetal condition usually defined as the excessive accumulation of fetal fluid within the fetal extravascular compartments and body cavities that manifests as edema, pleural and pericardial effusion and ascites. It is the end-stage of a wide variety of disorders. The cause may be immunologic (immune hydrops fetalis, IHF) or non immunologic (non-immune hydrops fetalis, NIHF), depending on the presence or absence of maternal antibodies against fetal red cell antigens (ABO incompatibility or rhesus (Rh) incompatibility).
http://linkedlifedata.com/resource/umls/id/C0020305, http://purl.obolibrary.org/obo/NCIT_C84767, http://identifiers.org/snomedct/276508000, http://purl.obolibrary.org/obo/Orphanet_1041, http://identifiers.org/mesh/D015160
fetal anasarca, hydrops fetalis, generalized fetal edema, HF, fetal hydrops, hydrops fetalis (disease)
familial non-immune hydrops fetalis, hydrops fetalis nonimmune, idiopathic hydrops fetalis, fetal edema
MONDO:0015193