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Infant, Premature, Diseases
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Infant, Premature, Diseases
Tree Number(s)
C16.614.521
Unique ID
D007235
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D007235
Annotation
add
INFANT, PREMATURE
Scope Note
Diseases that occur in
PREMATURE INFANTS
.
Entry Version
INFANT PREMATURE DIS
NLM Classification #
WS 410
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2015/12/16
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
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)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Infant, Newborn, Diseases [C16.614]
Amniotic Band Syndrome [C16.614.042]
Anemia, Neonatal [C16.614.053]
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]
Bronchopulmonary Dysplasia [C16.614.521.125]
Leukomalacia, Periventricular [C16.614.521.450]
Respiratory Distress Syndrome, Newborn [C16.614.521.563]
Retinopathy of Prematurity [C16.614.521.731]
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]
OEIS Complex [C16.614.660]
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]
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Infant, Premature, Diseases
Preferred
Concept UI
M0011290
Scope Note
Diseases that occur in
PREMATURE INFANTS
.
Terms
Infant, Premature, Diseases
Preferred Term
Term UI
T021691
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1966)
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