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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
muscular dystrophy +     
Adult-Onset Muscular Dystrophy with Leukoencephalopathy 
Alpha-B Crystallinopathy with Cataract 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
Bassoe Syndrome 
Becker muscular dystrophy +   
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
congenital muscular dystrophy +   
distal myopathy +   
A heterogeneous group of genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive.
Duchenne muscular dystrophy +   
Emery-Dreifuss muscular dystrophy +   
facioscapulohumeral muscular dystrophy +   
glycogen storage disease VII  
limb-girdle muscular dystrophy +   
Muscular Dystrophy, Animal +   
Muscular Dystrophy, Barnes Type 
Muscular Dystrophy, Cardiac Type 
Muscular Dystrophy, Mabry Type 
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries 
Myofibrillar Myopathy, ZASP-Related  
Myopathy with Abnormal Lipid Metabolism  
MYOPATHY, SCAPULOHUMEROPERONEAL  
myotonic disease +   
oculopharyngeal muscular dystrophy +   
Oculopharyngodistal Myopathy 
Progressive Muscular Dystrophy, Pectorodorsal 
rigid spine muscular dystrophy 1  
scapuloperoneal myopathy +   
Vacuolar Neuromyopathy 

Synonyms
Exact Synonyms: DISTAL MUSCLE WEAKNESS ;   Distal Muscular Dystrophies ;   distal muscular dystrophy ;   distal myopathy, Markesbery Griggs type ;   distal myopathy, early-onset, autosomal dominant ;   distal myopathy, late hereditary
Primary IDs: MESH:D049310
Alternate IDs: RDO:0002338
Xrefs: NCI:C84675 ;   ORDO:399086 ;   ORDO:399096 ;   ORDO:5448 ;   ORDO:63273
Definition Sources: MESH:D049310, https://rarediseases.org/rare-diseases/distal-myopathy/

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.