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DO Term : X-linked spinal muscular atrophy 2 [DOID:0111827] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A spinal muscular atrophy characterized by neonatal onset of severe hypotonia, areflexia, and multiple congenital contractures associated with loss of anterior horn cells and infantile death that has_material_basis_in hemizygous mutation in the UBA1 gene on chromosome Xp11.3.
  • synonyms:
  • X-linked spinal muscular atrophy type 2,
  • OMIM:301830,
  • infantile-onset X-linked spinal muscular atrophy,
  • 301830,
  • SMAX2,
  • UMLS_CUI:C1844934,
  • spinal muscular atrophy with arthrogryposis,
  • GARD:8521,
  • ORDO:1145,
  • X-linked distal arthrogryposis multiplex congenita,
  • MESH:C535380,
  • SNOMEDCT_US_2023_03_01:719836007
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