Phenotypes associated with the disease facioscapulohumeral muscular dystrophy 4, digenic (OMIM:619478, an entry in Online Mendelian Inheritance in Man):
- Upper limb muscle weakness (HP:0003484, a Human Phenotype Ontology term): Weakness of the muscles of the arms. Evidence: PCS. (PMID:27153398)
- Adult onset (HP:0003581, a Human Phenotype Ontology term): Onset of disease manifestations in adulthood, defined here as at the age of 16 years or later. Evidence: PCS. (PMID:27153398)
- Digenic inheritance (HP:0010984, a Human Phenotype Ontology term): A type of multifactorial inheritance governed by the simultaneous action of two gene loci. Evidence: PCS. (PMID:27153398)
- Weakness of facial musculature (HP:0030319, a Human Phenotype Ontology term): Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve). Evidence: PCS. (PMID:27153398)