Distal lower limb muscle weakness

Symptom Information:

Symptom ID: HPO:0009053
Synonyms:
Distal muscle weakness in lower limbs [HPO:0009053]
Muscle weakness, lower limb, distal [HPO:0009053]
Distal lower limb muscle weakness [OMIM:Distal lower limb muscle weakness]
Muscle weakness, lower limb, distal [OMIM:Muscle weakness, lower limb, distal]
Quality:
Cross references:
OMIM: "Distal lower limb muscle weakness" [OMIM:Distal lower limb muscle weakness]
OMIM: "Muscle weakness, lower limb, distal" [OMIM:Muscle weakness, lower limb, distal]
Is a (Direct Parents):
HPO         Distal muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Distal muscle weakness(HPO:0002460)
                   Distal lower limb muscle weakness(HPO:0009053)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
Autosomal recessive spastic paraplegia type 39 (Orphanet:139480)
Autosomal recessive spastic paraplegia type 43 (Orphanet:320370)
Behr syndrome (Orphanet:1239)
Cap myopathy (Orphanet:171881)
Charcot-Marie-Tooth disease type 4H (Orphanet:99954)
Distal hereditary motor neuropathy type 2 (Orphanet:139525)
Distal spinal muscular atrophy type 3 (Orphanet:139547)
NEMALINE MYOPATHY 1 (OMIM:609284)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB (OMIM:608634)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC (OMIM:613376)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)