Distal lower limb amyotrophy

Symptom Information:

Symptom ID: HPO:0008944
Synonyms:
Lower leg amyotrophy [HPO:0008944]
Lower limb atrophy [HPO:0008944]
Lower limb muscle hypotrophy [HPO:0008944]
Muscle atrophy, lower limb, distal [HPO:0008944]
Lower limb atrophy [OMIM:Lower limb atrophy]
Lower limb muscle hypotrophy [OMIM:Lower limb muscle hypotrophy]
Muscle atrophy, lower limb, distal [OMIM:Muscle atrophy, lower limb, distal]
Quality:
Cross references:
OMIM: "Lower limb atrophy" [OMIM:Lower limb atrophy]
OMIM: "Lower limb muscle hypotrophy" [OMIM:Lower limb muscle hypotrophy]
OMIM: "Muscle atrophy, lower limb, distal" [OMIM:Muscle atrophy, lower limb, distal]
Is a (Direct Parents):
HPO         Lower limb amyotrophy
HPO         Distal amyotrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Distal amyotrophy(HPO:0003693)
                   Distal lower limb amyotrophy(HPO:0008944)
                Lower limb amyotrophy(HPO:0007210)
                   Distal lower limb amyotrophy(HPO:0008944)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
Behr syndrome (Orphanet:1239)
Cap myopathy (Orphanet:171881)
Charcot-Marie-Tooth disease type 4H (Orphanet:99954)
Distal myopathy with posterior leg and anterior hand involvement (Orphanet:63273)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
NEMALINE MYOPATHY 1 (OMIM:609284)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)