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Showing Results for "list of rare diseases-c"


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Protein C deficiency (Disease)
; http://clotconnect.wordpress.com/2011/06/15/protein-c-deficiency/. Accessed 9/20/2011. Do you know of a review article? We want to hear from you. You can help advance rare disease research! You can help, deficiency Categories: Blood Diseases; Congenital and Genetic Diseases; Musculoskeletal Diseases Subtypes: Autosomal recessive protein C deficiency Summary Summary Listen Protein C deficiency is a disorder ...

Hemoglobin C disease (Disease)
Disease European Network for Rare and Congenital Anaemias (ENERCA) University of Barcelona Red Cell Pathology Unit C/Villarroel, 170 - 08036 Barcelona España Telephone: (34) 93 451 5950 Fax: (34) 93, to explore the biology of this condition. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable ...

Developmental dysphasia familial (Disease)
Hopkins University School of Medicine. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database, the services they offer. Inclusion on this list is not an endorsement by GARD. Organizations Supporting this Disease Childhood Apraxia of Speech Association of North America (CASANA) Cardello Building ...

Lupus erythematosus tumidus (Disease)
: Intermittent cutaneous lupus; Tumid lupus erythematosus Categories: Skin Diseases Subtypes: Cutaneous lupus erythematosus Summary Summary Listen Tumid erythematosus lupus is considered a rare type of chronic, Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. News & Events News & Events Listen News Rare Disease Day at NIH ...

Corpus callosum agenesis double urinary collecting (Disease)
offer. Inclusion on this list is not an endorsement by GARD. Organizations Supporting this Disease National Organization of Disorders of the Corpus Callosum PMB 363 18032-C Lemon Drive Yorba Linda, CA, on rare diseases and orphan drugs. Access to this database is free of charge. News & Events News & Events Listen News Rare Disease Day at NIH 2021 March 1, 2021 GARD Answers GARD Answers Listen ...

Autosomal dominant intermediate Charcot-Marie-Tooth (Disease)
biology of this condition. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. News & Events News & Events Listen, Living With Listen Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease ...

Autosomal recessive protein C deficiency (Disease)
Hopkins University School of Medicine. Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. News & Events News &, ; Thrombophilia due to protein C deficiency, autosomal recessive See More Categories: Blood Diseases; Congenital and Genetic Diseases; Musculoskeletal Diseases This disease is grouped under: Protein C deficiency ...

Cytochrome c oxidase deficiency (Disease)
Start MedlinePlus Genetics contains information on Cytochrome c oxidase deficiency. This website is maintained by the National Library of Medicine. The National Organization for Rare Disorders (NORD) has, Oxidase Deficiency. NORD. 2015; http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/1088/viewAbstract. Accessed 4/17/2013. Cytochrome c oxidase deficiency. Genetics Home Reference ...

Mast cell activation syndrome (Disease)
. Where to Start The Mast Cell Disease Society provides information about mast cell diseases, including Mast cell activation syndrome. Selected Full-Text Journal Articles Valent P, Akin C, Bonadonna P, et, ://medcraveonline.com/MOJI/MOJI-02-00032.pdf. Do you know of a review article? We want to hear from you. You can help advance rare disease research! You can help advance rare disease research! Find out how with the NCATS ...

Monoclonal mast cell activation syndrome (Disease)
Feedback Other Names: Monoclonal MCAD; MMAS Summary Summary Listen Monoclonal mast cell activation syndrome (MMAS) is a rare immunological disorder characterized by recurrent episodes of allergy, flushing, cell diseases, including Monoclonal mast cell activation syndrome. In-Depth Information Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database ...

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