FSHMD1A (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 2489 |
| Gene name | - |
| Gene symbol | FSHMD1A |
| Synonyms (NCBI Gene) |
FMDFSHDFSHD1AFSHMD
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| Chromosome | 4 |
| Chromosome location | 4q35 |
| Summary | Facioscapulohumeral muscular dystrophy (FSHD) is a common hereditary disease of muscle. Patients with FSHD have a chromosomal rearrangement within the subtelomeric region of chromosome 4 (4q35). This region is composed mainly of a polymorphic repeat struc |
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Related Genes
Genes most often co-reported with FSHMD1A across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to FSHMD1A (see Related Genes above), that are NOT already directly curated for FSHMD1A itself -- a lead worth checking, not a confirmed association.
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