Aliases: IGF1A, IGFI, IGF-I, IGF.
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 |
|---|---|---|
| Growth Hormone Insensitivity Syndrome | causative germline |
mechanism: Reduced IGF-1 Production and Action
subtype: IGF1 Deficiency
scoped to subtype: IGF1 Deficiency
|
| IGF1 Deficiency | causative germline |
mechanism: IGF1 Loss of Function
|
| Ewing Sarcoma | no genetic record |
mechanism: IGF-1/YAP1 Developmental Cooperation
discussion: (unnamed)
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.