Difficulty walking

Symptom Information:

Symptom ID: HPO:0002355
Synonyms:
Difficulty in walking [HPO:0002355]
Difficulty in walking [OMIM:Difficulty in walking]
Difficulty walking [OMIM:Difficulty walking]
Walking difficulties [OMIM:Walking difficulties]
Quality:
Cross references:
OMIM: "Difficulty in walking" [OMIM:Difficulty in walking]
OMIM: "Difficulty walking" [OMIM:Difficulty walking]
OMIM: "Walking difficulties" [OMIM:Walking difficulties]
Is a (Direct Parents):
HPO         Functional motor problems
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)
                   Difficulty walking(HPO:0002355)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Functional motor problems(HPO:0004302)
                Difficulty walking(HPO:0002355)
MedDRA:
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)