Mucopolysaccharidosis type VII (MPS VII) is a very rare lysosomal storage disease belonging to the group of mucopolysaccharidoses. [ Orphanet:584 ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:0007096 (Orphanet-shared)
  • UMLS:C0085132 (Orphanet:584)
  • MESH:D016538 (Orphanet:584)
  • NCIT:C84903 (MONDO:equivalentTo)
  • Orphanet:584 (OMIM:253220)
  • ICD10:E76.29 (DOID:12803)
  • ICD10:E76.2 (Orphanet:584)
  • MedDRA:10056893 (Orphanet:584)
  • OMIM:253220 (Orphanet:584)
  • SCTID:43916004 (MONDO:equivalentTo)
  • DOID:12803 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
MPSVII [ Orphanet:584 ]

abbreviation
MPS7 [ https://omim.org/entry/253220 MONDO:Lexical Orphanet:584 ]

closeMatch

http://identifiers.org/snomedct/124470009

definition

Mucopolysaccharidosis type VII (MPS VII) is a very rare lysosomal storage disease belonging to the group of mucopolysaccharidoses.

exactMatch

http://purl.obolibrary.org/obo/NCIT_C84903

http://purl.obolibrary.org/obo/DOID_12803

http://linkedlifedata.com/resource/umls/id/C0085132

http://identifiers.org/meddra/10056893

http://identifiers.org/omim/253220

http://identifiers.org/snomedct/43916004

http://identifiers.org/mesh/D016538

http://www.orpha.net/ORDO/Orphanet_584

has exact synonym

MPS VII - Sly syndrome

Sly disease

beta-glucuronidase deficiency

MPS7

deficiency of beta-glucuronidase

MPSVII

mucopolysaccharidosis type VII

mucopolysaccharidosis VII

Sly syndrome

Beta-glucuronidase deficiency

mucopolysaccharidosis, mps-VII

has related synonym

Gus deficiency

MPS VII

Gusb deficiency

MPS 7

MPS VII - mucopolysaccharidosis VII

mucopolysaccharidosis, type VII

gusb deficiency

mucopolysaccharidosis, type 7

id

MONDO:0009662