1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | A Charcot-Marie-Tooth disease X-linked that has_material_basis_in loss-of-function mutation in the PRPS1 gene on chromosome Xq22. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |