- Differential Diagnosis
- Diseases
- Drugs
- More
-
- Try building your search one term at a time, and be as specific as you can! Search term example: "chronic cough".
- Do not enter multiple findings such as "anemia, chronic cough, weight loss, vomiting" all at the same time.
- After selecting your term from the search results a list of possible diagnoses will be generated. If the list is too long, you will be able to narrow it down by entering additional terms.
- Do not enter values such as "heart rhythm 110" or "sodium 125", instead use "tachycardia" or "hyponatremia".
Sign-in (or register) to check out the new features we've just launched!
Differential Diagnosis For Spells/Episodes of weakness: Metabolic, Storage Disorders
List of current finding(s):
Spells/Episodes of weakness
- Trauma Causes (1)
- Infectious Disorders (Specific Agent) (1)
- Infected organ, Abscesses (1)
- Neoplastic Disorders (4)
- Allergic, Collagen, Auto-Immune Disorders (4)
- Metabolic, Storage Disorders (14)
- Biochemical Disorders (7)
- Congenital, Developmental Disorders (3)
- Hereditary, Familial, Genetic Disorders (8)
- Usage, Degenerative, Necrosis, Age Related Disorders (1)
- Relational, Mental, Psychiatric Disorders (10)
- Anatomic, Foreign Body, Structural Disorders (3)
- Arteriosclerotic, Vascular, Venous Disorders (12)
- Functional, Physiologic Variant Disorders (1)
- Vegetative, Autonomic, Endocrine Disorders (42)
- Reference to Organ System (6)
- Eponymic, Esoteric Disorders (1)
- Pathophysiologic (2)
- Heirarchical Major Groups (2)
- Drugs (2)
- Synonyms (2)
- Definition
- External Links Related to Spells/Episodes of weakness
- Metabolic, Storage Disorders:
- Diabetes mellitus, poorly controlled
- Diabetes mellitus
- Diabetic autonomic neuropathy syndrome
- Glucose 6 PD deficiency
- Porphyria, acute intermittent
- Cytochrome C Oxidase Deficiency/COX Complex Defect
- French-Canadian type COX mitochondrial defect
- Infantile mitochondrial myopathy/Cox defect
- LCHAD/Long chain OH-CoA dehydrogenase def
- MCAD/Medium chain OH-CoA Dehydrogenase def
- VLCHAD/Very Long chain OH-CoA dehydrogenase def
- Fructose intolerance, hereditary
- McArdle's syndrome
- Urea cycle/metabolic disorder
This site is designed primarily as a reminder system for use by qualified physicians and other medical professionals. By using this site you understand and accept that DiagnosisPro.com shall not be used as a diagnostic decision-making system and must not be used to make a clinical diagnosis or replace or overrule a licensed health care professional's judgment or clinical diagnosis (full terms of use). This site complies with the HONcode standard for trustworthy health information: verify here.
© 2013 MedTech USA, Inc. (last modified on 06/19/13)
