Waddling gait
Symptom Information:
Symptom ID: | HPO:0002515 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |