 |
|
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 |
| Brain Diseases, Metabolic, Inborn | Legal notice |
Other terms
Encephalopathies, Metabolic, Inborn,Inborn Errors of Metabolism, Brain,Metabolic Diseases, Inborn, Brain,Inborn Metabolic Brain Disorders,Inborn Metabolic Disorders, Brain,Metabolic Brain Diseases, Inborn,Metabolic Brain Syndrome, Inborn,Brain Syndrome, Metabolic, Inborn,Inborn Metabolic Brain Diseases,Central Nervous System Inborn Metabolic Diseases,Metabolic Disorders, CNS, Inborn,Metabolic Diseases, Inborn, Central Nervous System,Central Nervous System Inborn Metabolic Disorders,CNS Metabolic Disorders, Inborn,Brain Diseases, Metabolic, Inherited,Familial Metabolic Brain Diseases,Familial Metabolic Disorders, Brain,Metabolic Disorders, Familial, Brain,Inherited Metabolic Disorders, Brain,Metabolic Brain Diseases, Familial,Metabolic Brain Diseases, Inherited,Metabolic Disorders, Brain, Inherited,Brain Diseases, Metabolic, Familial,Inherited Metabolic Brain Diseases
Description
Brain Diseases, Metabolic, Inborn: Brain disorders resulting from inborn metabolic errors, primarily from enzymatic defects which lead to substrate accumulation, product reduction, or increase in toxic metabolites through alternate pathways. The majority of these conditions are familial, however spontaneous mutation may also occur in utero.
Pervious tree
Next tree
- Galactosemias
- Hartnup Disease
- Hepatolenticular Degeneration
- Homocystinuria
- Menkes Kinky Hair Syndrome
- Leigh Disease
- Lesch-Nyhan Syndrome
- Maple Syrup Urine Disease
- Oculocerebrorenal Syndrome
- Phenylketonurias
- Pyruvate Carboxylase Deficiency Disease
- Pyruvate Dehydrogenase Complex Deficiency Disease
- MELAS Syndrome
- MERRF Syndrome
- Peroxisomal Disorders
- Lysosomal Storage Diseases, Nervous System
- Hyperglycinemia, Nonketotic
- Hyperlysinemias
- Tyrosinemias
- Cerebral Amyloid Angiopathy, Familial
- Urea Cycle Disorders, Inborn
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.