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DO Term : epidermolysis bullosa simplex with muscular dystrophy [DOID:0090017] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An syndrome characterized by early childhood onset of progressive muscular dystrophy and blistering skin changes and that has_material_basis_in homozygous or compound heterozygous mutation in the PLEC gene on chromosome 8q24.
  • synonyms:
  • ORDO:257,
  • OMIM:226670,
  • ICD10CM:Q81.0,
  • limb-girdle muscular dystrophy with epidermolysis bullosa simplex,
  • epidermolysis bullosa simplex and limb-girdle muscular dystrophy,
  • 226670
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Ontology Term --> Direct children

Ontology Term --> Direct parents