Gowers sign

Symptom Information:

Symptom ID: HPO:0003391
Synonyms:
Gowers sign [HPO:0003391]
Positive Gower sign [HPO:0003391]
Positive Gowers sign [HPO:0003391]
Gower sign [OMIM:Gower sign]
Gowers sign [OMIM:Gowers sign]
Positive Gowers sign [OMIM:Positive Gowers sign]
Gowers sign (in some patients) [OMIM:Gowers sign (in some patients)]
Quality:
Cross references:
OMIM: "Gower sign" [OMIM:Gower sign]
OMIM: "Gowers sign" [OMIM:Gowers sign]
OMIM: "Positive Gowers sign" [OMIM:Positive Gowers sign]
OMIM: "Gowers sign (in some patients)" [OMIM:Gowers sign (in some patients)]
Is a (Direct Parents):
HPO         Proximal muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Proximal muscle weakness(HPO:0003701)
                   Gowers sign(HPO:0003391)
MedDRA:
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

Arginine:glycine amidinotransferase deficiency (Orphanet:35704)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal dominant limb-girdle muscular dystrophy type 1C (Orphanet:265)
Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet:34516)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Autosomal recessive limb-girdle muscular dystrophy type 2F (Orphanet:219)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Autosomal recessive limb-girdle muscular dystrophy type 2M (Orphanet:206554)
Autosomal recessive limb-girdle muscular dystrophy type 2O (Orphanet:206564)
Autosomal recessive limb-girdle muscular dystrophy type 2P (Orphanet:280333)
Autosomal recessive limb-girdle muscular dystrophy type 2Q (Orphanet:254361)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect (Orphanet:280671)
Congenital muscular dystrophy type 1B (Orphanet:98893)
Congenital myasthenic syndromes with glycosylation defect (Orphanet:353327)
Duchenne muscular dystrophy (Orphanet:98896)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 (OMIM:616094)
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616326)
MYASTHENIC SYNDROME, CONGENITAL, 12 (OMIM:610542)
MYASTHENIC SYNDROME, CONGENITAL, 14 (OMIM:616228)
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL (OMIM:608930)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616325)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Mitochondrial DNA depletion syndrome, myopathic form (Orphanet:254875)
Mitochondrial myopathy - lactic acidosis - deafness (Orphanet:2597)
Myopathy due to myoadenylate deaminase deficiency (OMIM:615511)
NEMALINE MYOPATHY 4 (OMIM:609285)
NEMALINE MYOPATHY 7 (OMIM:610687)
Neutral lipid storage myopathy (Orphanet:98908)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
Scheie syndrome (Orphanet:93474)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)