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mucopolysaccharidosis type 4

Go to external page http://purl.obolibrary.org/obo/MONDO_0018938

Mucopolysaccharidosis type IV (MPS IV) is a lysosomal storage disease belonging to the group of mucopolysaccharidoses, and characterized by spondylo-epiphyso-metaphyseal dysplasia. It exists in two forms, A and B. [ Orphanet:582 ]

Synonyms: MPS4 mucopolysaccharidosis type IV mucopolysaccharidosis IV Morquio syndrome Morquio disease mucopolysaccharidosis type 4 mucopolysaccharidosis, MPS-IV deficiency of chondroitinsulphatase MPSIV

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C61263 (MONDO:equivalentTo)
  • DOID:12804 (MONDO:equivalentTo)
  • NORD:1455 (MONDO:NORD)
  • UMLS:C0026707 (Orphanet:582/e)
  • Orphanet:582 (MONDO:equivalentTo)
  • MedDRA:10028095 (Orphanet:582/e)
  • SCTID:378007 (MONDO:equivalentTo)
  • GARD:12562 (Orphanet:582)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare

closeMatch

http://identifiers.org/meddra/10028095

exactMatch

http://identifiers.org/snomedct/378007

http://purl.obolibrary.org/obo/DOID_12804

http://linkedlifedata.com/resource/umls/id/C0026707

http://www.orpha.net/ORDO/Orphanet_582

http://purl.obolibrary.org/obo/NCIT_C61263

has narrow synonym

Osteochondrodystrophy

mucopolysaccharidosis type IVA

mucopolysaccharidosis type IVB

mucopolysaccharidosis, MPS-IV-A

chondroosteodystrophy

Morquio syndrome A

galactosamine-6-sulfatase deficiency

Morquio A disease

deficiency of N-acetylgalactosamine-6-sulphatase

MPS IV - Morquio syndrome B

MPS IV - Morquio syndrome A

id

MONDO:0018938