HSCR5 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 404720 |
| Gene name | - |
| Gene symbol | HSCR5 |
| Synonyms (NCBI Gene) |
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| Chromosome | 9 |
| Chromosome location | 9q31 |
| Summary | The disorder described by Hirschsprung (1888) and known as Hirschsprung disease or aganglionic megacolon is characterized by congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointesti |
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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 HSCR5 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to HSCR5 (see Related Genes above), that are NOT already directly curated for HSCR5 itself -- a lead worth checking, not a confirmed association.
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