 |
|
Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
| Enter a medical term |
| Hyperlipoproteinemia Type II | Legal notice |
Other terms
Hyperlipoproteinemia Type IIs,Hyperbetalipoproteinemia,Hyperbetalipoproteinemias,Hyper-beta-Lipoproteinemia,Hyper beta Lipoproteinemia,Hyper-beta-Lipoproteinemias,Hypercholesterolemia, Familial,Familial Hypercholesterolemia,Familial Hypercholesterolemias,Hypercholesterolemias, Familial,Hyperlipoproteinemia Type 2,2, Hyperlipoproteinemia Type,2s, Hyperlipoproteinemia Type,Hyperlipoproteinemia Type 2s,Type 2, Hyperlipoproteinemia,Type 2s, Hyperlipoproteinemia,Hyper-Low Density Lipoproteinemia,Density Lipoproteinemia, Hyper-Low,Density Lipoproteinemias, Hyper-Low,Hyper Low Density Lipoproteinemia,Hyper-Low Density Lipoproteinemias,Lipoproteinemia, Hyper-Low Density,Lipoproteinemias, Hyper-Low Density,Hypercholesterolemia, Essential,Essential Hypercholesterolemia,Essential Hypercholesterolemias,Hypercholesterolemias, Essential,Hyperlipoproteinemia Type IIb,Hyperlipoproteinemia Type IIbs,Familial Combined Hyperlipoproteinemia,Combined Hyperlipoproteinemia, Familial,Combined Hyperlipoproteinemias, Familial,Familial Combined Hyperlipoproteinemias,Hyperlipoproteinemia, Familial Combined,Hyperlipoproteinemias, Familial Combined,Hypercholesterolemia, Autosomal Dominant, Type B,Apolipoprotein B-100, Familial Ligand-Defective,Apolipoprotein B 100, Familial Ligand Defective,Hyperlipoproteinemia Type IIa,Hyperlipoproteinemia Type IIas,LDL Receptor Disorder,Disorder, LDL Receptor,Disorders, LDL Receptor,LDL Receptor Disorders,Receptor Disorder, LDL,Receptor Disorders, LDL,Hypercholesterolemia, Autosomal Dominant,Autosomal Dominant Hypercholesterolemia,Autosomal Dominant Hypercholesterolemias,Dominant Hypercholesterolemia, Autosomal,Dominant Hypercholesterolemias, Autosomal,Hypercholesterolemias, Autosomal Dominant
Description
Hyperlipoproteinemia Type II: A group of familial disorders characterized by elevated circulating cholesterol contained in either LOW-DENSITY LIPOPROTEINS alone or also in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins).
Pervious tree
Next tree
Other locations in tree
Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
Neither the United States Government, nor any of its agencies, contractors, subcontractors or employees makes any warranties, expressed or implied, with respect to data contained in the database, and, furthermore, assumes no legal liability for any party's use, or the results of such use, of any part of the database.
You will not assert any proprietary rights to any portion of the database, or represent the database or any part thereof to anyone as other than a United States Government database.
The MeSH data carry an international copyright outside the United States, its Territories or Possessions. These terms and conditions are in effect as long as the user retains any of the MeSH data obtained from this site.