Previous symbols: DDX37. Aliases: KIAA1517, MGC4322, MGC2695, Dhr1.
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 |
|---|---|---|
| 46,XY complete gonadal dysgenesis | causative germline |
mechanism: DHX37-related gonadal-development failure
subtype: DHX37-related complete gonadal dysgenesis
|
| 46,XY partial gonadal dysgenesis | causative germline |
mechanism: DHX37 sequence alteration; Reduced DHX37 protein abundance
subtype: DHX37-related PGD
|
| 46,XY Sex Reversal 11 | causative germline |
mechanism: DHX37 Missense Variation
variant: DHX37 p.Arg308Gln; DHX37 p.Arg334Trp; DHX37 p.Arg390His; DHX37 p.Arg674Trp; DHX37 p.Gly478Arg
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.