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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
ACANTHOCYTOSIS  
Adenosine Triphosphate, Elevated, of Erythrocytes  
Amniotic Band Syndrome +  
anemia +   
asphyxia neonatorum +   
Autoimmune Diseases +   
benign neonatal seizures +   
Birth Injuries +   
blood coagulation disease +   
blood group incompatibility +   
blood protein disease +   
bone marrow disease +   
Caffey disease +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
chorioamnionitis +   
cocoon syndrome  
Colic 
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis 
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Diabetic Embryopathy  
Echogenic Bowel 
Familial Macrocytosis  
fetal alcohol spectrum disorder +   
fetal erythroblastosis +   
A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN.
Fetal Growth Retardation +   
Fetal Hypoxia  
Fetal Macrosomia +   
Fetal Nutrition Disorders  
Graft vs Host Disease  
Hematologic Neoplasms +   
hemorrhagic disease +   
hereditary elliptocytosis +   
hydrophthalmos +   
Hyperglycinemia, Transient Neonatal 
Hyperparathyroidism, Neonatal Severe Primary  
hypersensitivity reaction disease +   
hypochromic microcytic anemia +   
ichthyosis +   
IMAGEI Syndrome  
Immune Reconstitution Inflammatory Syndrome 
Immune Response to Synthetic Polypeptide--IrGAT 
Immune Suppression 
immune system cancer +   
Immunoproliferative Disorders +   
IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES  
Infantile Hypercalcemia +   
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
Kabuki syndrome +   
leukocyte disease +   
lymphatic system disease +   
Lymphoblastic Transformation, Inhibition of 
meconium aspiration syndrome  
Meconium Ileus  
Megaduodenum  
membranoproliferative glomerulonephritis +   
methemoglobinemia +   
Mobius syndrome +   
Monocyte Chemotactic Disorder 
Multiple Pterygium Syndrome, Lethal Type  
neonatal abstinence syndrome 
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes mellitus +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica 
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis  
NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA  
Neutrophil Chemotactic Response, Abnormal 
Nuchal Cord 
ophthalmia neonatorum 
otulipenia  
pancytopenia +   
persistent fetal circulation syndrome  
polycythemia +   
Posttransfusion Purpura  
Pregnancy Complications, Hematologic 
Preleukemias 
Premature Infant Diseases +   
primary immunodeficiency disease +   
Pseudo-TORCH Syndrome 2  
Pyelectasis 
Radiation Sensitivity of Natural Killer Activity 
Rh deficiency syndrome  
Rh isoimmunization  
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
severe combined immunodeficiency +   
sulfhemoglobinemia +  
thanatophoric dysplasia +   
Thrombocytopenic Purpura +   
Tn polyagglutination syndrome  
Transfusion Reaction  
transient neonatal thrombocytopenia 
Transplant Rejection +   
umbilical hernia +   
vitamin K deficiency bleeding  
Wolman disease +   
 Hydrops Fetalis +   
 kernicterus +   

Synonyms
Exact Synonyms: EF - Erythroblastosis foetalis ;   Erythroblastosis Fetali ;   Erythroblastosis Fetalis ;   Fetal Erythroblastoses ;   Hemolytic Disease of Newborn ;   Newborn Hemolytic Disease ;   Newborn Hemolytic Diseases ;   haemolytic disease due to rhesus isoimmunisation ;   rhesus isoimmunisation of the newborn
Related Synonyms: RADIN BLOOD GROUP
Primary IDs: MESH:D004899
Alternate IDs: RDO:0005530
Xrefs: NCI:C101304
Definition Sources: MESH:D004899

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.