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GENE - TERM ANNOTATION REPORT

RGD ID: 736976
Species: Homo sapiens
RGD Object: Gene
Symbol: DMD
Name: dystrophin
Acc ID: HP:0003457
Term: EMG abnormality
Definition: Abnormal results of investigations using electromyography (EMG).
Definition Source(s): https://orcid.org/0000-0002-0736-9199, PMID:15961866, PMID:18751841
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
DMD IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: EMG abnormality

PMID:16770791 PMID:17253928 PMID:25007885 PMID:25741868 PMID:28492532 PMID:34106991
DMD IAGP 8699517HPO ORPHA:154
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