Ullrich congenital muscular dystrophy https://www.malacards.org/card/ullrich_congenital_muscular_dystrophy_1a icd11.foundation:1011547453 late onset scleroatonic familial myopathy (subtype) Ullrich disease DOID:0050558 UMLS:C4551860 Orphanet:75840 MEDGEN:1642667 MESH:C537521 OMIMPS:254090 NCIT:C123438 Ullrich congenital muscular dystrophy (UCMD) is characterized by early-onset, generalized and slowly progressive muscle weakness, multiple proximal joint contractures, marked hypermobility of the distal joints and normal intelligence. scleroatonic muscular dystrophy MONDO:0000355 congenital muscular dystrophy, Ullrich type NANDO:2200862 NANDO:1200215 Ullrich scleroatonic muscular dystrophy SCTID:240062007 scleroatonic Ullrich disease GARD:0004769 UCMD congenital muscular dystrophy congenital myopathy