obsolete congenital muscular dystrophy merosin-positive

Term ID

DOID:0110638

Synonyms

Definition

A congenital muscular dystrophy characterized by autosomal recessive inheritance of generalized muscle weakness and hypotonia without arthrogryposis or central nervous system involvement that has_material_basis_in mutation in the chromosome region 4p16.3. (3)

References

Obsolete

true

Secondary ID:

Merged into

congenital myasthenic syndrome 10

Ontology

  ( DOID:0110638 )