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DO Term : mucopolysaccharidosis type IIIB [DOID:0111394] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.
  • synonyms:
  • 252920,
  • GARD:7072,
  • Mucopoly-saccharidosis type 3B,
  • MPS3B,
  • MESH:D009084,
  • Mucopolysaccharidosis type 3B,
  • OMIM:252920,
  • mucopolysaccharidosis type IIIB (Sanfilippo B),
  • ICD10CM:E76.22,
  • Sanfilippo syndrome type B,
  • MPSIIIB,
  • SNOMEDCT_US_2023_03_01:254071004,
  • ORDO:79270,
  • NCI:C84898,
  • NAGLU deficiency,
  • UMLS_CUI:C0086648,
  • N-acetyl-alpha-glucosaminidase deficiency
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