Hypotrophy of the small hand muscles

Symptom Information:

Symptom ID: HPO:0006006
Synonyms:
Hypotrophy of the small hand muscles [OMIM:Hypotrophy of the small hand muscles]
Quality:
Cross references:
OMIM: "Hypotrophy of the small hand muscles" [OMIM:Hypotrophy of the small hand muscles]
Is a (Direct Parents):
HPO         Abnormality of the musculature of the hand
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the musculature of the hand(HPO:0001421)
                            Hypotrophy of the small hand muscles(HPO:0006006)
                   Abnormality of the musculature of the limbs(HPO:0009127)
                      Abnormality of the musculature of the upper limbs(HPO:0001446)
                         Abnormality of the musculature of the hand(HPO:0001421)
                            Hypotrophy of the small hand muscles(HPO:0006006)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of the musculature of the limbs(HPO:0009127)
             Abnormality of the musculature of the upper limbs(HPO:0001446)
                Abnormality of the musculature of the hand(HPO:0001421)
                   Hypotrophy of the small hand muscles(HPO:0006006)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Koolen-De Vries syndrome (Orphanet:96169)