Difficulty walking
Symptom Information:
Symptom ID: | HPO:0002355 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Functional motor problems(HPO:0004302) Difficulty walking(HPO:0002355) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Gait disturbance(HPO:0001288) Difficulty walking(HPO:0002355) MedDRA: |
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Database Frequency: | 61 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Autosomal dominant Charcot-Marie-Tooth disease type 2N | (Orphanet:228174) |
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy type 2F | (Orphanet:219) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 28 | (Orphanet:101008) |
Autosomal recessive spastic paraplegia type 32 | (Orphanet:171622) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Brain-lung-thyroid syndrome | (Orphanet:209905) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q | (OMIM:615025) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Charcot-Marie-Tooth disease type 4G | (Orphanet:99953) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Distal hereditary motor neuropathy type 7 | (Orphanet:139589) |
Distal myopathy, Welander type | (Orphanet:603) |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3 | (OMIM:613608) |
FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION | (OMIM:227250) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Lower motor neuron syndrome with late-adult onset | (Orphanet:276435) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYASTHENIC SYNDROME, CONGENITAL, 17 | (OMIM:616304) |
MYASTHENIC SYNDROME, CONGENITAL, 18 | (OMIM:616330) |
MYOPATHY, CENTRONUCLEAR, 1 | (OMIM:160150) |
Monosomy 5p | (Orphanet:281) |
NEMALINE MYOPATHY 4 | (OMIM:609285) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB | (OMIM:608634) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID | (OMIM:615575) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA | (OMIM:158580) |
Neutral lipid storage myopathy | (Orphanet:98908) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
Progressive demyelinating neuropathy with bilateral striatal necrosis | (Orphanet:217396) |
Progressive myoclonic epilepsy type 6 | (Orphanet:280620) |
Progressive pseudorheumatoid arthropathy of childhood | (Orphanet:1159) |
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE | (OMIM:615685) |
SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT | (OMIM:616282) |
STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL | (OMIM:500003) |
Spinocerebellar ataxia type 35 | (Orphanet:276193) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B | (OMIM:600081) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |