Intrinsic hand muscle atrophy

Symptom Information:

Symptom ID: HPO:0008954
Synonyms:
Atrophy of the intrinsic hand muscles [OMIM,du]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Hand muscle atrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                   Hand muscle atrophy(HPO:0009130)
                      Intrinsic hand muscle atrophy(HPO:0008954)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Upper limb amyotrophy(HPO:0009129)
                   Distal upper limb amyotrophy(HPO:0007149)
                      Hand muscle atrophy(HPO:0009130)
                         Intrinsic hand muscle atrophy(HPO:0008954)
                Distal amyotrophy(HPO:0003693)
                   Distal upper limb amyotrophy(HPO:0007149)
                      Hand muscle atrophy(HPO:0009130)
                         Intrinsic hand muscle atrophy(HPO:0008954)
       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 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)
                            Hand muscle atrophy(HPO:0009130)
                               Intrinsic hand muscle atrophy(HPO:0008954)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the musculature of the hand(HPO:0001421)
                            Hand muscle atrophy(HPO:0009130)
                               Intrinsic hand muscle atrophy(HPO:0008954)
                      Upper limb amyotrophy(HPO:0009129)
                         Distal upper limb amyotrophy(HPO:0007149)
                            Hand muscle atrophy(HPO:0009130)
                               Intrinsic hand muscle atrophy(HPO:0008954)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive spastic paraplegia type 43 (Orphanet:320370)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED (OMIM:302900)