mucopolysaccharidosis type 4B https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/mucopolysaccharidosis_type_ivb icd11.foundation:1479415032 MPS IVB mucopolysaccharidosis type IVB NANDO:2201179 Beta-D-galactosidase deficiency Morquio disease type B MPS IV B SCTID:238044004 OMIM:253010 GARD:0003786 Orphanet:309310 MPS 4B UMLS:C0086652 NANDO:1200107 MONDO:0009660 MPSIVB DOID:0111392 NCIT:C84902 MPS4B MEDGEN:43376 ICD10CM:E76.211 Morquio syndrome B A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme beta galactosidase. It is characterized by skeletal dysplasia and short stature. mucopolysaccharidosis type 4 lysosomal storage disease with skeletal involvement obsolete_mucopolysaccharidosis type 4B