Mild proximal muscle weakness (<10% of patients)

Symptom Information:

Symptom ID: OMIM : No Id available
Muscle weakness, proximal, mild [OMIM:Muscle weakness, proximal, mild]
Proximal muscle weakness, mild [OMIM:Proximal muscle weakness, mild]
Cross references:
OMIM: "Mild proximal muscle weakness (<10% of patients)" [OMIM:Mild proximal muscle weakness (<10% of patients)]
OMIM: "Muscle weakness, proximal, mild" [OMIM:Muscle weakness, proximal, mild]
OMIM: "Proximal muscle weakness, mild" [OMIM:Proximal muscle weakness, mild]
Is a (Direct Parents):
Is a (Whole tree): HPO:
Database Frequency: 5 / 7739

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2N (Orphanet:206559)
Cardiomyopathy, dilated, 1X (OMIM:611615)
Gyrate atrophy of choroid and retina (Orphanet:414)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)