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DO Term : muscular dystrophy-dystroglycanopathy type B6 [DOID:0110637] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with mental retardation and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LARGE gene on chromosome 22q12.
  • synonyms:
  • ICD10CM:G71.2,
  • congenital muscular dystrophy LARGE-related,
  • 608840,
  • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6,
  • MDC1D,
  • ORDO:98894,
  • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6,
  • MDDGB6,
  • congenital muscular dystrophy type 1D,
  • OMIM:608840
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