Previous symbols: MLS. Aliases: CCHL.
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 |
|---|---|---|
| Histiocytoid Cardiomyopathy | disputed | |
| Linear Skin Defects with Multiple Congenital Anomalies 1 | causative |
mechanism: HCCS Holocytochrome c-Type Synthase Deficiency
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.