about
P1050
IgG4- related disease: an orphan disease with many facesOrphan diseases of the nose and paranasal sinuses: Pathogenesis - clinic - therapyThe ABCC6 Transporter as a Paradigm for Networking from an Orphan Disease to Complex DisordersGroup 5 Pulmonary Hypertension: The Orphan's Orphan Disease.Orphan disease gains second treatment option.Carcinoma of Unknown Primary - an Orphan Disease?Database identifies FDA-approved drugs with potential to be repurposed for treatment of orphan diseases.A vertex similarity-based framework to discover and rank orphan disease-related genes.Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan disease.Hereditary angioedema: new hopes for an orphan disease.Development of a provisional model to improve transitional care for female adolescents with a rare genital malformation as an example for orphan diseases.The cystic fibrosis therapeutics development network (CF TDN): a paradigm of a clinical trials network for genetic and orphan diseases.Random forest classification of etiologies for an orphan disease.Health information, what happens when there isn't any? Information literacy and the challenges for rare and orphan diseases.Childhood tuberculosis: no longer an orphan disease?Bronchiectasis: not an orphan disease in the East.Therapeutic options for variant renal cancer: a true orphan disease.The utility of tumour necrosis factor blockade in orphan diseases.Fibrinous tumor of the pleura: an orphan disease lost in translation.DIGNiFI: Discovering causative genes for orphan diseases using protein-protein interaction networks.The Food and Drug Administration's Office of Orphan Products Development: incentives, grants, and special designations speed therapies for orphan diseases.Pyruvate dehydrogenase phosphatase deficiency: orphan disease or an under-diagnosed condition?Chorismate synthase: an attractive target for drug development against orphan diseases.Inhibitor development in haemophilia B: an orphan disease in need of attention.Analysis of cystic fibrosis-associated P67L CFTR illustrates barriers to personalized therapeutics for orphan diseasesErdheim-Chester disease, moving away from the orphan diseases: A case report.From an orphan disease to a generalized molecular mechanism: PTPN11 loss-of-function mutations in the pathogenesis of metachondromatosisDrug development for orphan diseases in the context of personalized medicine.Drug repositioning for orphan diseases.Two coronary "orphan" diseases in search of clinical consideration: coronary syndromes x and y.Mechanisms of pleural involvement in orphan diseases.A generalizable pre-clinical research approach for orphan disease therapyGene, stem cell, and future therapies for orphan diseases.Primary ciliary dyskinesia, an orphan disease.Severe asthma in adults: an orphan disease?Financing drug discovery for orphan diseases.Hodgkin's Lymphoma in Older Patients: an Orphan Disease?Familial amyloidosis: great progress for an orphan disease.The international diffuse intrinsic pontine glioma registry: an infrastructure to accelerate collaborative research for an orphan disease.Prioritization of orphan disease-causing genes using topological feature and GO similarity between proteins in interaction networks.
P921
Q21146649-FA238C91-06C1-49D3-97E0-E4A9D5456414Q26771869-E57E5943-F7EA-4BAE-BD01-E125ABFCB7F2Q26781908-79472D58-A501-4E1F-89C0-5435B64E5F88Q30248872-7D7E6286-D7B9-45C4-9C2B-6BA683B53C68Q33383070-B75B73FA-8E17-4A65-94A8-822EE45006ABQ34096326-18F2DF4C-0902-4886-9FB0-2F513B10F046Q34167318-9FA8E2DB-C5BB-486A-B28E-D1817249386BQ34529478-28C494DB-8321-4E77-9345-EF0A29993F16Q34547335-03DEDD25-6E99-480F-A4EE-FFDC0FA3673CQ34603480-8157DA12-A36E-4DA4-AFBA-BB0ED353F549Q34722362-57953A69-3DD8-4149-80E0-AF526E2E4A71Q35012439-83152036-6F8A-44F2-90A4-88AD1E3DB6BBQ35027782-D486C8E1-43E0-41E9-AE09-71C64D7B11C1Q35231519-C09F4D23-1629-43E6-B0F6-3AAF00032F58Q35719391-68C942CA-2C36-47A9-849E-2A6E3056B457Q35795055-7628083E-9FAE-4473-AFCC-E6E357B44B24Q35901631-F149FEB6-729F-4BE9-A6FC-98384D0B1D6EQ35915996-E0EC79DE-D9E6-4BDA-9CEA-3EC5379E2F57Q36287656-725E5DEB-F2C5-4E7F-9685-980618BBFF4EQ36329373-B02560C9-E115-4270-A9E0-FEB02A28D2EBQ36351572-E3A05BD3-47A5-48AA-8F96-76BEE3AB790EQ36436080-9CD2DF85-DB39-4F6C-A45D-2BDD4C940BE5Q36755781-A1850A52-5A38-4237-B80A-2E6FADF205BAQ36872038-582AFF58-A083-4049-B603-62EAF614D748Q37269585-AFB84774-BB68-4FEF-8A93-1431F06C02C9Q37496942-703E0200-808B-4119-AE69-B83D535802BAQ37590300-FA09F0F6-0A81-43BB-B8CC-F9121A55DC4CQ37636722-FE7B5871-0658-429D-82A2-940B1C25628AQ37866927-C0695634-7528-4EAF-81D0-05E9A0826BBFQ37925002-5C2374D3-B5BB-4EFD-ABBC-EF54841515A3Q37976241-BCA4E48E-06F7-443E-BEEE-DE3D5058A918Q38019219-C33C4CA8-F125-4A75-8934-1310FCE3EF83Q38022126-1D727238-4FF1-4F4E-9C12-D4FE5AEAD4EDQ38025037-5B822D2C-AFB4-4A6B-B755-98E433970BBBQ38038714-4E9B5712-E59D-4EFB-8004-745D8560F8D4Q38165615-9D54DC98-B624-4051-9E1A-67A6B56C70CCQ38232075-B801E9DC-6CE0-4FAE-A724-4A91FFD2B9EAQ38249071-4394D472-467B-43F5-9847-2A863DCC1866Q38374138-10EA6D5F-70B2-4442-BCC9-908E5358D97DQ38422071-7776EAFB-837D-46A2-B517-95E68A50A27F
P921
description
Krankheit
@de
malattia
@it
name
Orphan diseases
@en
Vzácná onemocnění
@cs
maladie orpheline
@fr
type
label
Orphan diseases
@en
Vzácná onemocnění
@cs
maladie orpheline
@fr
prefLabel
Orphan diseases
@en
Vzácná onemocnění
@cs
maladie orpheline
@fr
P279
P31
P3417
Orphan-Diseases