WormMine: OntologyRelation

• Relationship: is_a
• Parent Term . Identifier: DOID:630
• Child Term . Identifier: DOID:0110489
• Direct: false
• Redundant: false

1 Child Term

• Identifier: DOID:0110489
• Name: autosomal recessive nonsyndromic deafness 30
• Description: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1.

1 Parent Term

• Identifier: DOID:630
• Name: genetic disease
• Description: A disease that has_material_basis_in genetic variations in the human genome.