developmental anomaly of metabolic origin glycoproteinosis mucolipidosis https://www.malacards.org/card/mucolipidosis NCIT:C61267 UMLS:C0026697 A group of inherited lysosomal storage diseases characterized by accumulation of lipids and carbohydrates in the tissues, resulting in mental disabilities and skeletal malformations. icd11.foundation:714623911 GARD:0018975 Orphanet:79212 DOID:0080488 SCTID:70528007 MESH:D009081 MONDO:0019248 MEDGEN:7731