WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:66
• Child Term . Identifier: DOID:0110280
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0110280
• Name: autosomal recessive limb-girdle muscular dystrophy type 2F
• Description: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the sarcoglycan-delta gene (SGCD).

1 Parent Term

• Identifier: DOID:66
• Name: muscle tissue disease
• Description: A muscular disease located in the muscle tissue.