Waddling gait

Symptom Information:

Symptom ID: HPO:0002515
Synonyms:
'Waddling' gait [HPO:0002515]
'Waddling' gait [OMIM:'Waddling' gait]
Quality:
Cross references:
OMIM: "'Waddling' gait" [OMIM:'Waddling' gait]
Is a (Direct Parents):
HPO         Gait disturbance
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Gait disturbance(HPO:0001288)
                   Waddling gait(HPO:0002515)
MedDRA:
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Autosomal dominant limb-girdle muscular dystrophy type 1D (Orphanet:34516)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Autosomal recessive limb-girdle muscular dystrophy type 2M (Orphanet:206554)
Autosomal recessive lower motor neuron disease with childhood onset (Orphanet:206580)
CHST3-related skeletal dysplasia (Orphanet:263463)
Camurati-Engelmann disease (Orphanet:1328)
Charcot-Marie-Tooth disease type 4H (Orphanet:99954)
Childhood-onset hypophosphatasia (Orphanet:247667)
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect (Orphanet:280671)
Congenital myasthenic syndromes with glycosylation defect (Orphanet:353327)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
Czech dysplasia, metatarsal type (Orphanet:137678)
DPM3-CDG (Orphanet:263494)
Desbuquois syndrome (Orphanet:1425)
Duchenne muscular dystrophy (Orphanet:98896)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Faciocardiorenal syndrome (Orphanet:1973)
Familial osteochondritis dissecans (Orphanet:251262)
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia (Orphanet:79091)
MYASTHENIC SYNDROME, CONGENITAL, 14 (OMIM:616228)
MYOPATHY, MYOSIN STORAGE (OMIM:608358)
Metaphyseal anadysplasia (Orphanet:1040)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Multiple epiphyseal dysplasia due to collagen 9 anomaly (Orphanet:166002)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Multiple synostoses syndrome (Orphanet:3237)
Muscle filaminopathy (Orphanet:171445)
Myopathy due to myoadenylate deaminase deficiency (OMIM:615511)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 4 (OMIM:609285)
Nemaline myopathy (Orphanet:607)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Pseudoachondroplasia (Orphanet:750)
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT (OMIM:300695)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Singleton-Merten dysplasia (Orphanet:85191)
Smith-McCort dysplasia (Orphanet:178355)
Spheroid body myopathy (Orphanet:268129)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia, MacDermot type (Orphanet:163668)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED (OMIM:310300)