Human genes for congenital muscular dystrophy-dystroglycanopathy A7
Congenital muscular dystrophy-dystroglycanopathy A7 [DOID:0111234]
A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in ISPD on 7p21.2-p21.1.
Synonyms: congenital muscular dystrophy-dystroglycanopathy A7, congenital muscular dystrophydystroglycanopathy A7, DOID:0111234, congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A7, MDDGA7 ...