Muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Muscle weakness, symmetric, proximal (lower limbs more affected than upper limbs) due to motor neuronopathy [OMIM:Muscle weakness, symmetric, proximal (lower limbs more affected than upper limbs) due to motor neuronopathy]
Muscle weakness, symmetric, proximal due to motor neuronopathy [OMIM:Muscle weakness, symmetric, proximal due to motor neuronopathy]
Quality:
Cross references:
OMIM: "Muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy" [OMIM:Muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy]
OMIM: "Muscle weakness, symmetric, proximal (lower limbs more affected than upper limbs) due to motor neuronopathy" [OMIM:Muscle weakness, symmetric, proximal (lower limbs more affected than upper limbs) due to motor neuronopathy]
OMIM: "Muscle weakness, symmetric, proximal due to motor neuronopathy" [OMIM:Muscle weakness, symmetric, proximal due to motor neuronopathy]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Proximal spinal muscular atrophy type 1 (Orphanet:83330)
Proximal spinal muscular atrophy type 2 (Orphanet:83418)
Proximal spinal muscular atrophy type 3 (Orphanet:83419)
Proximal spinal muscular atrophy type 4 (Orphanet:83420)