First dorsal interossei muscle atrophy

Symptom Information:

Symptom ID: HPO:0003426
Synonyms:
First dorsal interossei muscle atrophy [OMIM:First dorsal interossei muscle atrophy]
Quality:
Cross references:
OMIM: "First dorsal interossei muscle atrophy" [OMIM:First dorsal interossei muscle atrophy]
Is a (Direct Parents):
HPO         Interosseus muscle atrophy
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)
                   Interosseus muscle atrophy(HPO:0007181)
                      First dorsal interossei muscle atrophy(HPO:0003426)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2D (Orphanet:99938)
Autosomal dominant spastic paraplegia type 17 (Orphanet:100998)
Autosomal dominant spastic paraplegia type 38 (Orphanet:171617)
Distal hereditary motor neuropathy type 5 (Orphanet:139536)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA (OMIM:600794)