Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
facioscapulohumeral muscular dystrophy 3
Summary
- Synonym
-
- FSHD3
- facioscapulohumeral muscular dystrophy type 3
- Definition
- A facioscapulohumeral muscular dystrophy characterized by adult onset of proximal muscle weakness affecting the face, neck, scapular muscles, and upper and lower limbs that has_material_basis_in the combination of a homozygous mutation in the LRIF1 gene on chromosome 1p13 and presence of a haplotype on chromosome 4 that is permissive for DUX4 expression.
- Super Class
- digenic disease facioscapulohumeral muscular dystrophy
External Links
- Disease Ontology
- DOID:0060917
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003202 | Skeletal muscle atrophy |
| HP:0008046 | Abnormal retinal vascular morphology |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0100540 | Palpebral edema |
| HP:0003307 | Hyperlordosis |
| HP:0000298 | Mask-like facies |
| HP:0003457 | EMG abnormality |
| HP:0000499 | Abnormal eyelash morphology |
| HP:0030680 | Abnormal cardiovascular system morphology |
| HP:0003236 | Elevated circulating creatine kinase concentration |
