WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:17
• Child Term . Identifier: DOID:0110196
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0110196
• Name: Charcot-Marie-Tooth disease type 4G
• Description: A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.

1 Parent Term

• Identifier: DOID:17
• Name: musculoskeletal system disease
• Description: A disease of anatomical entity that occurs in the muscular and/or skeletal system.