facioscapulohumeral muscular dystrophy https://github.com/monarch-initiative/mondo/issues/1631 https://github.com/monarch-initiative/mondo/issues/5658 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/facioscapulohumeral_muscular_dystrophy_1 MEDGEN:65956 facioscapulohumeral dystrophy SCTID:399091004 NORD:1116 FSHD MONDO:0001347 FSH dystrophy NCIT:C84704 MedDRA:10064087 GARD:0009941 MESH:D020391 UMLS:C0238288 NANDO:2200859 DOID:11727 ICD10CM:G71.02 An autosomal dominant disorder affecting the skeletal muscles of the face, scapula, and upper arm. Patients present with muscle weakness in these anatomic areas. The muscle weakness eventually spreads to other skeletal muscles as well. NANDO:1200491 OMIMPS:158900 facioscapulohumeral muscular dystrophy facioscapulohumeral myopathy icd11.foundation:621965073 Orphanet:269 progressive muscular dystrophy telomere syndrome