Steppage gait
Symptom Information:
Symptom ID: | HPO:0003376 | ||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Gait disturbance(HPO:0001288) Steppage gait(HPO:0003376) MedDRA: |
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Database Frequency: | 41 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 | (Orphanet:99946) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant Charcot-Marie-Tooth disease type 2F | (Orphanet:99940) |
Autosomal dominant Charcot-Marie-Tooth disease type 2G | (Orphanet:99941) |
Autosomal dominant Charcot-Marie-Tooth disease type 2I | (Orphanet:99942) |
Autosomal dominant Charcot-Marie-Tooth disease type 2J | (Orphanet:99943) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | (Orphanet:100043) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F | (Orphanet:352670) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | (Orphanet:254334) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S | (OMIM:616155) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T | (OMIM:616233) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U | (OMIM:616280) |
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D | (OMIM:616039) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1D | (Orphanet:101084) |
Charcot-Marie-Tooth disease type 1E | (Orphanet:90658) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Charcot-Marie-Tooth disease type 2H | (Orphanet:101102) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Distal myopathy, Welander type | (Orphanet:603) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Giant axonal neuropathy | (Orphanet:643) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
MYOPATHY, DISTAL, INFANTILE-ONSET | (OMIM:160300) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT | (OMIM:300695) |
Spinocerebellar ataxia type 1 with axonal neuropathy | (Orphanet:94124) |
Tibial muscular dystrophy | (Orphanet:609) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked Charcot-Marie-Tooth disease type 6 | (Orphanet:352675) |