Aliases: SLIM1, KYO-T, bA535K18.1, FHL1B, XMPMA, FLH1A, MGC111107.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Emery-Dreifuss Muscular Dystrophy | causative |
mechanism: FHL1 Deficiency and Impaired Sarcomere Assembly
subtype: EDMD6
scoped to subtype: EDMD6
|
| Myofibrillar Myopathy | causative |
mechanism: Z-Disc and Chaperone Protein Variant
subtype: FHL1-Related
scoped to subtype: FHL1-Related
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.