National Institutes of Health. Visit the website 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, Gliomatosis cerebri Title Categories: Nervous System Diseases Summary Summary Listen Gliomatosis cerebri is a type of malignant (cancerous) brain tumor called a glioblastoma that develops from a ...
Panuveitis Title Other Names: Inflammation of the whole uveal tract; Total uveitis; Diffuse uveitis Categories: Eye diseases Summary Summary Listen Panuveitis is inflammation of all layers of the, familial cases of uveitis have been reported, it is very rare. The few cases that have been reported may represent the familial occurrence of underlying conditions that are associated with uveitis (e.g ...
ascites See More Categories: Digestive Diseases; Rare Cancers Summary Summary Listen Pseudomyxoma peritonei (PMP) is a rare disease characterized by the presence of mucin in the abdominal (peritoneal, and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition. Orphanet is a European reference portal for information on rare diseases and orphan drugs ...
health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. Orphanet is a European reference portal for information on rare diseases and orphan drugs, ; EIEE14; Malignant migrating partial epilepsy of infancy; Migrating partial seizures in infancy See More Categories: Congenital and Genetic Diseases; Nervous System Diseases Summary Summary Listen Malignant ...
researchers. OMIM is maintained by Johns 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, : Blood Diseases; Congenital and Genetic Diseases; Metabolic disorders Summary Summary Listen Orotic aciduria type I (OA1), also known as hereditary orotic aciduria, is a rare condition characterized by ...
Kaposiform lymphangiomatosis Title Categories: Blood Diseases Summary Summary Listen Kaposiform lymphangiomatosis (KLA) is a rare type of tumor and vascular malformation that results from the, these resources with a medical professional. In-Depth Information Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. GARD ...
with cold urticaria, a distinct red and swollen rash will generally develop within minutes of exposure. Additional blood tests may be done to determine if there are associated diseases. Diagnostic, someone with cold urticaria include: Allergist Immunologist Last updated: 5/11/2020 Statistics Statistics Listen Cold urticaria is rare and the exact number of people that have it is unknown. The incidence ...
Double inferior vena cava Title Not a rare disease Other Names: Double IVC Categories: Congenital and Genetic Diseases Summary Summary Listen Double inferior vena cava is a vein abnormality that is, /28145872. Mano A, Tatsumi T, Sakai H, Imoto Y, Nomura T, Nishikawa S, Takeda M, Kobara M, Yamagami T, Matsubara H. A case of deep venous thrombosis with a double inferior vena cava effectively treated by ...
compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the, Y, Nishi T, Mizuguchi K, Ishibashi M. Diabetic mastopathy of bilateral breasts in an elderly Japanese woman with type 2 diabetes: a case report and a review of the literature in Japan. Intern Med ...
include: Obstetrician/gynecologist Endocrinologist Dermatologist Last updated: 11/18/2020 Statistics Statistics Listen It can be difficult to estimate the exact number of people affected by a rare condition, and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National ...
