Hereditary Inflammatory Myopathies

X-LinkedImmune/AntibodyOMIM 249100

antibody/infmyop.htm#Hereditary Inflammatory Myopathies

Overview

From WUSTL Neuromuscular

Dystrophy FSH dystrophy LGD 2B ? LGD 2A: May be only myopathic groups ± eosinophils Inclusion Body Myositis: Familial Familial Idiopathic Inflammatory Myopathy Immune system disorders, Monogenic 140 IPEX: FOXP3 FPF (TRAPS): TNFRSF1A Familial Mediterranean Fever (FMF) : MEFV Familial cold autoinflammatory syndrome-1 (FCAS1) : NLRP3 Cryopyrin-Associated Periodic Syndrome (CINCA; NLRP3-AID) : NLRP3 Familial cold autoinflammatory syndrome-2 (FCAS2) : NLRP12 Hyper-IgD & Periodic fever syndrome (HIDS) : MVK 153 Yao : NOD2, IVS8+158 Blau (Granulomatous) : NOD2, Exon 4 Vasculitis, Autoinflammation, Im

OMIM Entries

OMIM #249100 OMIM #608107 OMIM #120100 OMIM #606416 OMIM #607115 OMIM #611762 OMIM #609648 OMIM #260920 OMIM #251170 OMIM #617321 OMIM #605956 OMIM #186580 OMIM #615688 OMIM #607575 OMIM #269200

External Resources

WUSTL Neuromuscular

Washington University Disease Center

OMIM

Online Mendelian Inheritance in Man

PubMed

Biomedical Literature

GeneReviews

NCBI Expert-Authored Reviews

Orphanet

Portal for Rare Diseases

NORD

National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.