Monomelic Amyotrophy(Hirayama disease) Explore Disorder's Alias
An Unknown mode(s) within the Neuromuscular disorders category
Candidate Gene Information
An Unknown mode(s) within the Neuromuscular disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | SLIT1/6585 | slit guidance ligand 1 | 10q24.1 | Chr10, NC_000010.11 (96998038..97185959, complement) |
187922 nt | 37 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GARD GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |