Oculopharyngodistal Myopathies (OPDM)

Muscular Dystrophy

musdist/peeom.html#Oculopharyngodistal Myopathies (OPDM)

Overview

From WUSTL Neuromuscular

OPDM1: LRP12 OPDM2: GIPC1 OPDM3 + Neurological: NOTCH2NLC OPDM4: RILPL1 OPDM5: ABCD3 OPDM: LOC642361/NUTM2B-AS1 Disease mechanism: GGC repeats Also see OPMD: PABP2 OPML1: LOC642361/NUTM2B-AS1 DNA repeat disorders

Related Conditions

Shared genes

FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A (FSHMD 1A)

DNMT3BLRIF1SMALL

HERPES ZOSTER (Varicella)

VZVDNAC6

Myopathic Tremor

AS1ANIMAL

Nuclei: Muscle Fibers

DNA

Oculopharyngeal Myopathy with Leukodystrophy (OPML1)

AS1

Vocal Cord & Pharyngeal Weakness (MPD2; VCPDM; ALS21; MSP5)

DNA

External Resources

WUSTL Neuromuscular

Washington University Disease Center

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.