Association Review
In brief
The association between ENSG00000266919 (Hsa-Mir-423) and Muscular Dystrophy, Duchenne Type is reported, supported by a single source.
Sources
1
Clinical variants
0
Symptoms
50
Compounds
0
Trials
0
Publications
1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.
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02
Provenance
Evidence and sources
1 source
Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.
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03
Muscular Dystrophy, Duchenne Type
The disorder
11 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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04
Phenotype
Clinical features
39 clinical features
The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.
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1 publication
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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06
Provenance
References & sources
7 references
Every source and publication cited across this dossier, as one numbered reference list.
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