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Showing Results for "list of rare diseases-d"


Filtered by: Type=Diseases;

Mucopolysaccharidosis type III (Disease)
guidelines for patients with rare diseases and for the anesthesiologists caring for them. The project is a collaborative effort of the German Society of Anesthesiology and Intensive Care, Orphanet, the, European Society of Pediatric Anesthesia, anesthetists and rare disease experts with the aim to contribute to patient safety. Research Research Listen Research helps us better understand diseases and can ...

Vogt-Koyanagi-Harada disease (Disease)
reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal articles that discuss, ://rarediseases.org/rare-diseases/vogt-koyanagi-harada-disease/. 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 ...

Ring chromosome 16 (Disease)
have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an, . Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic ...

Mucous membrane pemphigoid (Disease)
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 database of medical literature and lists, : Benign mucosal pemphigoid; Benign mucous membrane pemphigoid; Cicatricial pemphigoid disease Categories: Skin Diseases Summary Summary Listen Mucous membrane pemphigoid is a rare, chronic, blistering and ...

Astroblastoma (Disease)
astroblastoma Categories: Rare Cancers Summary Summary Listen Astroblastoma is a rare glial tumor usually located in the cerebral hemisphere of the brain.[1] It can occur in individuals of any age, but occurs, predominantly in children and young adults.[2] Signs and symptoms depend on the location and size of the tumor but most commonly include headaches and seizures.[1] Because these tumors are rare, there is little ...

Visual snow syndrome (Disease)
. National Organization for Rare Disorders (NORD). 2018; https://rarediseases.org/rare-diseases/visual-snow-syndrome/. Kondziella D, Olsen MH, Dreier JP. Prevalence of visual snow syndrome in the UK. Eur J, for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal articles that discuss Visual snow ...

D-glycericacidemia (Disease)
reference portal for information on rare diseases and orphan drugs.Orpha Number: 941DefinitionD-glyceric aciduria is a metabolic disorder characterized by D-glyceric acid excretion. It has been described in, 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 of medical literature and lists ...

Neuronal ceroid lipofuscinosis 10 (Disease)
reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal articles that discuss, is grouped under: Neuronal ceroid lipofuscinosis Summary Summary Listen Neuronal ceroid lipofuscinosis 10 (CLN10 disease) is a type of neuronal ceroid lipofuscinosis (NCL), a group of severe diseases ...

Neurodevelopmental disorder with severe motor impairment and absent language (Disease)
experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by, . It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. Selected Full-Text Journal Articles Lessel D, Schob C, Küry S, Reijnders ...

Post-transplant lymphoproliferative disease (Disease)
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. Selected Full-Text, : https://lymphoma-action.org.uk Do you know of an organization? We want to hear from you. Living With Living With Listen Living with a genetic or rare disease can impact the daily lives of patients and ...

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