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Anemia, Neonatal
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Anemia, Neonatal
Tree Number(s)
C15.378.050.363
C16.614.053
Unique ID
D000751
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000751
Annotation
check the tag
INFANT, NEWBORN
Scope Note
The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation.
Entry Term(s)
Anemia Neonatorum
NLM Classification #
WS 421
Previous Indexing
Anemia (1966-1967)
Infant, Newborn, Diseases (1966-1967)
Public MeSH Note
68
History Note
68
Date Established
1968/01/01
Date of Entry
1999/01/01
Revision Date
2023/02/26
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Anemia [C15.378.050]
Anemia, Aplastic [C15.378.050.085]
Anemia, Hemolytic [C15.378.050.141]
Anemia, Hypochromic [C15.378.050.196]
Anemia, Macrocytic [C15.378.050.252]
Anemia, Myelophthisic [C15.378.050.307]
Anemia, Neonatal [C15.378.050.363]
Fetofetal Transfusion [C15.378.050.363.344]
Fetomaternal Transfusion [C15.378.050.363.511]
Anemia, Refractory [C15.378.050.400]
Anemia, Sideroblastic [C15.378.050.419]
Red-Cell Aplasia, Pure [C15.378.050.750]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Infant, Newborn, Diseases [C16.614]
Amniotic Band Syndrome [C16.614.042]
Anemia, Neonatal [C16.614.053]
Fetofetal Transfusion [C16.614.053.344]
Fetomaternal Transfusion [C16.614.053.511]
Asphyxia Neonatorum [C16.614.092]
Birth Injuries [C16.614.131]
Colic [C16.614.166]
Congenital Bone Marrow Failure Syndromes [C16.614.183]
Congenital Hyperinsulinism [C16.614.200]
Cystic Fibrosis [C16.614.213]
Epilepsy, Benign Neonatal [C16.614.258]
Erythroblastosis, Fetal [C16.614.304]
Hernia, Umbilical [C16.614.378]
Hydrophthalmos [C16.614.438]
Hyperbilirubinemia, Neonatal [C16.614.451]
Hyperostosis, Cortical, Congenital [C16.614.465]
Ichthyosis [C16.614.492]
Infant, Premature, Diseases [C16.614.521]
Meconium Aspiration Syndrome [C16.614.580]
Mobius Syndrome [C16.614.595]
Neonatal Abstinence Syndrome [C16.614.610]
Neonatal Sepsis [C16.614.627]
Nystagmus, Congenital [C16.614.643]
Ophthalmia Neonatorum [C16.614.677]
Persistent Fetal Circulation Syndrome [C16.614.694]
Rothmund-Thomson Syndrome [C16.614.760]
Sclerema Neonatorum [C16.614.810]
Severe Combined Immunodeficiency [C16.614.815]
Syphilis, Congenital [C16.614.868]
Thanatophoric Dysplasia [C16.614.890]
Thrombocytopenia, Neonatal Alloimmune [C16.614.899]
Toxoplasmosis, Congenital [C16.614.909]
Vitamin K Deficiency Bleeding [C16.614.940]
Wolman Disease [C16.614.947]
Expand All
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Anemia, Neonatal
Preferred
Concept UI
M0001136
Scope Note
The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation.
Terms
Anemia, Neonatal
Preferred Term
Term UI
T002243
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1968)
Anemia Neonatorum
Term UI
T002244
Date
05/24/1993
LexicalTag
NON
ThesaurusID
NLM (1994)
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