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Lymphatic Abnormalities
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Lymphatic Abnormalities
Tree Number(s)
C15.604.451
C16.131.482
Unique ID
D044148
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D044148
Scope Note
Congenital or acquired structural abnormalities of the lymphatic system (
LYMPHOID TISSUE
) including the lymph vessels.
NLM Classification #
WH 720
Public MeSH Note
2004
History Note
2004
Date Established
2004/01/01
Date of Entry
2003/07/09
Revision Date
1955/01/01
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]
Lymphatic Diseases [C15.604]
Histiocytosis [C15.604.250]
Lymphadenitis [C15.604.315]
Lymphadenopathy [C15.604.338]
Lymphangiectasis [C15.604.360]
Lymphangitis [C15.604.406]
Lymphatic Abnormalities [C15.604.451]
22q11 Deletion Syndrome [C15.604.451.249]
Lymphangiectasis, Intestinal [C15.604.451.500]
Lymphedema [C15.604.496]
Lymphocele [C15.604.510]
Lymphoproliferative Disorders [C15.604.515]
Mucocutaneous Lymph Node Syndrome [C15.604.560]
Pseudolymphoma [C15.604.613]
Splenic Diseases [C15.604.744]
Thymus Hyperplasia [C15.604.816]
Thymus Neoplasms [C15.604.861]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
Chromosome Disorders [C16.131.260]
Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
Eye Abnormalities [C16.131.384]
Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
22q11 Deletion Syndrome [C16.131.482.249]
Lymphangiectasis, Intestinal [C16.131.482.500]
Musculoskeletal Abnormalities [C16.131.621]
Nervous System Malformations [C16.131.666]
Respiratory System Abnormalities [C16.131.740]
Situs Inversus [C16.131.810]
Skin Abnormalities [C16.131.831]
Stomatognathic System Abnormalities [C16.131.850]
Thyroid Dysgenesis [C16.131.894]
Urogenital Abnormalities [C16.131.939]
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Lymphatic Abnormalities
Preferred
Concept UI
M0444479
Scope Note
Congenital or acquired structural abnormalities of the lymphatic system (
LYMPHOID TISSUE
) including the lymph vessels.
Terms
Lymphatic Abnormalities
Preferred Term
Term UI
T529925
Date
01/08/2003
LexicalTag
NON
ThesaurusID
NLM (2004)
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