Steppage gait

Symptom Information:

Symptom ID: HPO:0003376
Synonyms:
Steppage gait [OMIM:Steppage gait]
'Steppage' gait [OMIM:'Steppage' gait]
Quality:
Cross references:
OMIM: "Steppage gait" [OMIM:Steppage gait]
OMIM: "'Steppage' gait" [OMIM:'Steppage' 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)
                   Steppage gait(HPO:0003376)
MedDRA:
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)