markerdb.ca

Marker DB

Is a freely available electronic database that attempts to consolidate information on all known clinical biomarkers into a single source. The database provides information such as: names and synonyms, associated conditions or pathogens, specificity and sensitivity, standard measurement values, measurement sources, variants, sequence information, molecular structure, FDA approval and references as well as links to other sources of information. Bacterial Infections and Mycoses. Skin and Connective Tissue.

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Marker DB | markerdb.ca Reviews

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Is a freely available electronic database that attempts to consolidate information on all known clinical biomarkers into a single source. The database provides information such as: names and synonyms, associated conditions or pathogens, specificity and sensitivity, standard measurement values, measurement sources, variants, sequence information, molecular structure, FDA approval and references as well as links to other sources of information. Bacterial Infections and Mycoses. Skin and Connective Tissue.

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1 downloads

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3 conditions

4 all markers

5 chemicals

6 genetic markers

7 proteins

8 karyotypes

9 chemical

10 genetic

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downloads,full site,conditions,all markers,chemicals,genetic markers,proteins,karyotypes,chemical,genetic,protein,karyotype,diagnostic,prognostic,predictive,exposure,monitoring,marker db,condition categories,autoimmune,cancer,cardiovascular,communication

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Marker DB | markerdb.ca Reviews

https://markerdb.ca

Is a freely available electronic database that attempts to consolidate information on all known clinical biomarkers into a single source. The database provides information such as: names and synonyms, associated conditions or pathogens, specificity and sensitivity, standard measurement values, measurement sources, variants, sequence information, molecular structure, FDA approval and references as well as links to other sources of information. Bacterial Infections and Mycoses. Skin and Connective Tissue.

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markerdb.ca

1

Marker DB

http://www.markerdb.ca/conditions/category/Digestive%20System

Achalasia Addisonianism Alacrima Syndrome. Adenomatous Polyposis Of The Colon. Bile Acid Malabsorption, Primary. Bile Acid Synthesis Defect. Biliary Cirrhosis, Primary. Blue Rubber Bleb Nevus. Budd Chiari Syndrome Membranous Obstruction Of Inferior Vena Cava, Included. Colorectal Adenomatous Polyposis, Autosomal Recessive. Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities. Desmoid Disease, Hereditary. Esophageal Cancer Esophageal Squamous Cell Carcinoma.

2

Marker DB

http://www.markerdb.ca/conditions/category/Communication

Asperger Syndrome, X Linked. Charcot Marie Tooth Disease And Deafness. Craniofacial Deafness Hand Syndrome. Diabetes Deafness Syndrome, Maternally Transmitted. Gonadal Dysgenesis, XX Type, With Deafness. Keratitis Ichthyosis Deafness Syndrome, Autosomal Dominant. Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X Linked. Speech Language Disorder 1. Bacterial Infections and Mycoses. Congenital, Hereditary, and Neonatal and Abnormalities. Female Urogenital and Pregnancy Complications.

3

Marker DB

http://www.markerdb.ca/categories/prognostic

Slow progression to Pulmanary Sarcoidosis. Slow progression to Kidney Disease. Slow progression to Pulmanary Sarcoidosis. Slow progression to Pulmanary Sarcoidosis. Slow progression to Pulmanary Sarcoidosis. Slow progression to Pulmanary Sarcoidosis. Slow progression to Kidney Disease. Slow progression to Pulmanary Sarcoidosis. Slow progression to Kidney Disease. Slow progression to Pulmanary Sarcoidosis. Slow progression to Pulmanary Sarcoidosis. Slow progression to Pulmanary Sarcoidosis.

4

Marker DB

http://www.markerdb.ca/conditions/category/Congenital,%20Hereditary,%20and%20Neonatal%20and%20Abnormalities

Congenital, Hereditary, and Neonatal and Abnormalities. 17-Beta Hydroxysteroid Dehydrogenase III Deficiency. 17-Beta Hydroxysteroid Dehydrogenase X Deficiency. 2-Methylbutyryl Co A Dehydrogenase Deficiency. 3-Methylcrotonyl Co A Carboxylase 1 Deficiency. 3-Methylcrotonyl Co A Carboxylase 2 Deficiency. 46,XX Gonadal Dysgenesis, Complete, Sry Positive. 46,XY Gonadal Dysgenesis, Complete Or Partial, DHH Related. 46,XY Gonadal Dysgenesis, Complete Or Partial, With 9p24.3 Deletion. Female Urogenital and Pregn...

5

Marker DB

http://www.markerdb.ca/conditions/category/Cutaneous

Aplasia Of Lacrimal And Salivary Glands. Ciliary Dyskinesia, Primary. Foveal Hypoplasia And Presenile Cataract Syndrome Foveal Hypoplasia, Isolated, Included. Ichthyosis, X Linked. Keratitis Ichthyosis Deafness Syndrome, Autosomal Dominant. Leiomyoma, Hereditary Multiple, Of Skin. Melanoma, Cutaneous Malignant. Noonan Syndrome Like Disorder With Loose Anagen Hair. Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, And Acne. Skin Fragility Woolly Hair Syndrome. Skin/Hair/Eye Pigmentation, Variation In, 1.

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The Human Metabolome Database (HMDB). The Toxin and Toxin Target Database (T3DB). Is a unique bioinformatics resource that combines detailed toxin data with comprehensive toxin target information. The database currently houses over 2900 toxins described by over 34 200 synonyms, including pollutants, pesticides, drugs, and food toxins, which are linked to over 1300 corresponding toxin target records. Altogether there are over 33 800 toxin, toxin target associations. The CSF Metabolome database. Is a freel...

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Marker DB

Is a freely available electronic database that attempts to consolidate information on all known clinical biomarkers into a single source. The database provides information such as: names and synonyms, associated conditions or pathogens, specificity and sensitivity, standard measurement values, measurement sources, variants, sequence information, molecular structure, FDA approval and references as well as links to other sources of information. Bacterial Infections and Mycoses. Skin and Connective Tissue.

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