Hand muscle atrophy

Symptom Information:

Symptom ID: HPO:0009130
Synonyms:
Amyotrophy involving the musculature of the hand [HPO:0009130]
Amyotrophy of hand muscles [HPO:0009130]
Hand muscle wasting [HPO:0009130]
Hand muscle wasting, bilateral [HPO:0009130]
Amyotrophy of hand muscles [OMIM:Amyotrophy of hand muscles]
Hand muscle atrophy [OMIM:Hand muscle atrophy]
Hand muscle wasting [OMIM:Hand muscle wasting]
Quality:
Cross references:
OMIM: "Amyotrophy of hand muscles" [OMIM:Amyotrophy of hand muscles]
OMIM: "Hand muscle atrophy" [OMIM:Hand muscle atrophy]
OMIM: "Hand muscle wasting" [OMIM:Hand muscle wasting]
Is a (Direct Parents):
HPO         Abnormality of the musculature of the hand
HPO         Distal upper limb 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)
                Upper limb amyotrophy(HPO:0009129)
                   Distal upper limb amyotrophy(HPO:0007149)
                      Hand muscle atrophy(HPO:0009130)
                Distal amyotrophy(HPO:0003693)
                   Distal upper limb amyotrophy(HPO:0007149)
                      Hand muscle atrophy(HPO:0009130)
          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)
       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)
                            Hand muscle atrophy(HPO:0009130)
                      Upper limb amyotrophy(HPO:0009129)
                         Distal upper limb amyotrophy(HPO:0007149)
                            Hand muscle atrophy(HPO:0009130)
                   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)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (OMIM:205100)
Autosomal dominant Charcot-Marie-Tooth disease type 2C (Orphanet:99937)
Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Juvenile amyotrophic lateral sclerosis (Orphanet:300605)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB (OMIM:607641)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Riboflavin transporter deficiency (Orphanet:97229)
SPINAL MUSCULAR ATROPHY, SEGMENTAL (OMIM:183020)
Spondyloepiphyseal dysplasia, Reardon type (Orphanet:163662)