1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110634 | congenital muscular dystrophy 1B | A congenital muscular dystrophy characterized by autosomal recessive inheritance of proximal muscle weakness, muscle hypertrophy, and early respiratory failure that has_material_basis_in variation in the chromosome region 1q42. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |
