Mucopolysaccharidosis type IV (MPS IV) is a lysosomal storage disease belonging to the group of mucopolysaccharidoses, and characterised by spondylo-epiphyso-metaphyseal dysplasia. It exists in two forms, A and B. [ Orphanet:582 ]
Term information
- UMLS:C0026707 (Orphanet:582)
- Orphanet:582 (MONDO:equivalentTo)
- ICD10:E76.210 (DOID:12804)
- NCIT:C61263 (MONDO:equivalentTo)
- DOID:12804 (MONDO:equivalentTo)
- MedDRA:10028095 (Orphanet:582)
- SCTID:378007 (MONDO:equivalentTo)
- ICD10:E76.2 (Orphanet:582)
- ICD10:E76.219 (DOID:12804)
- GARD:0012562 (Orphanet-shared)
ordo_disease
http://identifiers.org/snomedct/254074007
http://identifiers.org/snomedct/78856008
http://identifiers.org/snomedct/124449003
http://identifiers.org/snomedct/190936000
http://identifiers.org/snomedct/130197005
Mucopolysaccharidosis type IV (MPS IV) is a lysosomal storage disease belonging to the group of mucopolysaccharidoses, and characterised by spondylo-epiphyso-metaphyseal dysplasia. It exists in two forms, A and B.
http://identifiers.org/snomedct/378007
http://purl.obolibrary.org/obo/DOID_12804
http://linkedlifedata.com/resource/umls/id/C0026707
http://identifiers.org/meddra/10028095
http://www.orpha.net/ORDO/Orphanet_582
http://purl.obolibrary.org/obo/NCIT_C61263
http://identifiers.org/mesh/D009085
MPS4
mucopolysaccharidosis type IV
mucopolysaccharidosis IV
Morquio syndrome
Morquio disease
mucopolysaccharidosis type 4
mucopolysaccharidosis, MPS-IV
deficiency of chondroitinsulphatase
MPSIV
mucopolysaccharidosis type IVA
Osteochondrodystrophy
mucopolysaccharidosis type IVB
mucopolysaccharidosis, MPS-IV-A
chondroosteodystrophy
Morquio syndrome A
Morquio A disease
galactosamine-6-sulfatase deficiency
deficiency of N-acetylgalactosamine-6-sulphatase
MPS IV - Morquio syndrome B
MPS IV - Morquio syndrome A