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Ontology Browser

Term:
Miyoshi muscular dystrophy (DOID:0070198)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
distal myopathy +     
muscular atrophy +     
Allan-Herndon-Dudley syndrome  
amyotrophic lateral sclerosis type 21  
Arnold Stickler Bourne Syndrome 
distal muscular dystrophy 3 
distal muscular dystrophy 4  
distal muscular dystrophy Tateyama type  
distal muscular dystrophy with anterior tibial onset  
distal myopathy 1  
Distal Myopathy 5  
Facial Dysmorphism with Multiple Malformations +   
Furukawa Takagi Nakao Syndrome 
infantile-onset distal myopathy 
Jankovic Rivera Syndrome  
lethal congenital contracture syndrome 3  
Malignant Neurogenic Muscular Atrophy 
Miles-Carpenter syndrome  
Miyoshi muscular dystrophy +   
A distal muscular dystrophy characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood. (DO)
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
myofibrillar myopathy 9  
Nathalie Syndrome 
Nonaka Myopathy  
Primrose Syndrome  
Sarcopenia  
Thakker Donnai Syndrome 
tibial muscular dystrophy  
Welander Distal Myopathy, Swedish Type  

Synonyms
Exact Synonyms: Miyoshi distal myopathy ;   Miyoshi myopathy ;   distal muscular dystrophy, late onset, autosomal recessive
Primary IDs: MESH:C537480
Alternate IDs: DOID:9005765 ;   RDO:0003326
Xrefs: GARD:9676 ;   OMIM:PS254130 ;   ORDO:45448
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/3942856

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