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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Fetal Diseases +     
immune system disease +     
Infant, Newborn, Diseases +     
microcytic anemia +     
Abnormal Neutrophil Chemotactic Response 
allergic disease +   
Amniotic Band Syndrome +  
asphyxia neonatorum +   
autoimmune disease +   
benign neonatal seizures +   
Birth Injuries +   
Caffey disease +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
chorioamnionitis +   
Colic 
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis  
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Diabetic Embryopathy  
Echogenic Bowel 
fetal alcohol spectrum disorder +   
fetal encasement syndrome  
Fetal Growth Retardation +   
Fetal Hypoxia  
Fetal Inflammatory Response Syndrome  
Fetal Macrosomia +   
Fetal Nutrition Disorders  
graft-versus-host disease +   
Growth Hormone Insensitivity with Immune Dysregulation +   
hemolytic disease of the fetus +   
A microcytic anemia that is characterized by Rho(D) incompatibility, which may develop when a woman with Rh-negative blood is impregnated by an individual with Rh-positive blood and conceives a fetus with Rh-positive blood, sometimes resulting in hemolysis. (DO)
hydrophthalmos +   
Hyperparathyroidism, Neonatal Severe Primary  
hypersensitivity reaction disease +   
hypochromic microcytic anemia +   
ichthyosis +   
IMAGEI Syndrome  
Immune Reconstitution Inflammatory Syndrome 
Immune Suppression 
immune system cancer +   
Immunoproliferative Disorders +   
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
Infantile Hypercalcemia +   
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
Inhibition of Lymphoblastic Transformation 
lymphatic system disease +   
meconium aspiration syndrome  
Meconium Ileus  
Megaduodenum  
membranoproliferative glomerulonephritis +   
Moebius 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  
Nuchal Cord 
ophthalmia neonatorum 
persistent fetal circulation syndrome  
Posttransfusion Purpura  
Premature Infant Diseases +   
primary immunodeficiency disease +   
Pseudo-TORCH Syndrome 2  
Pseudo-TORCH Syndrome 3  
Pyelectasis 
Radiation Sensitivity of Natural Killer Activity 
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
severe combined immunodeficiency +   
sideroblastic anemia +   
thalassemia +   
thanatophoric dysplasia +   
Thrombocytopenic Purpura +   
Transfusion Reaction +   
Transient Neonatal Hyperglycinemia 
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 ;   Hemolytic disease of the fetus and newborn ;   alloimmune HDFN ;   fetal erythroblastosis ;   haemolytic disease due to rhesus isoimmunisation ;   hemolytic disease of newborn ;   newborn hemolytic disease ;   newborn hemolytic diseases
Related Synonyms: BLOOD GROUP--KIDD SYSTEM ;   KELL K/K BLOOD GROUP POLYMORPHISM ;   RADIN BLOOD GROUP
Xrefs: EFO:1000937 ;   ICD10CM:P55 ;   ICD10CM:P55.9 ;   ICD9CM:773 ;   MESH:D004899 ;   MONDO:0006760 ;   NCI:C101304
Definition Sources: https://www.ncbi.nlm.nih.gov/books/NBK557423/ "DO" "DO", MESH:D004899

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