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Vitamin K Deficiency Bleeding
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Vitamin K Deficiency Bleeding
Tree Number(s)
C15.378.100.920.360
C15.378.463.841.464
C16.614.940
C18.654.422.360
C18.654.521.500.133.912.360
Unique ID
D006475
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006475
Annotation
do not confuse with
HEMOLYTIC DISEASE OF NEWBORN
see
ERYTHROBLASTOSIS, FETAL
Scope Note
Hemorrhage caused by vitamin K deficiency.
Entry Term(s)
Hemorrhagic Disease of Newborn
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2010/06/25
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]
Blood Coagulation Disorders [C15.378.100]
Vitamin K Deficiency [C15.378.100.920]
Vitamin K Deficiency Bleeding [C15.378.100.920.360]
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Hemorrhagic Disorders [C15.378.463]
Vitamin K Deficiency [C15.378.463.841]
Vitamin K Deficiency Bleeding [C15.378.463.841.464]
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]
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]
Nutritional and Metabolic Diseases [C18]
Nutrition Disorders [C18.654]
Infant Nutrition Disorders [C18.654.422]
Vitamin K Deficiency Bleeding [C18.654.422.360]
Nutritional and Metabolic Diseases [C18]
Nutrition Disorders [C18.654]
Malnutrition [C18.654.521]
Deficiency Diseases [C18.654.521.500]
Avitaminosis [C18.654.521.500.133]
Vitamin K Deficiency [C18.654.521.500.133.912]
Vitamin K Deficiency Bleeding [C18.654.521.500.133.912.360]
Expand All
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Vitamin K Deficiency Bleeding
Preferred
Concept UI
M0010158
Scope Note
Hemorrhage caused by vitamin K deficiency.
Terms
Vitamin K Deficiency Bleeding
Preferred Term
Term UI
T731220
Date
12/05/2008
LexicalTag
NON
ThesaurusID
NLM (2010)
Hemorrhagic Disease of Newborn
Related
Concept UI
M0536624
Scope Note
Neonatal nasogastric or intracranial hemorrhage caused by vitamin K deficiency.
Terms
Hemorrhagic Disease of Newborn
Preferred Term
Term UI
T019534
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1966)
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