Shuffling gait

Symptom Information:

Symptom ID: HPO:0002362
Synonyms:
Shuffling gait [OMIM:Shuffling gait]
Quality:
Cross references:
OMIM: "Shuffling gait" [OMIM:Shuffling 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)
                   Shuffling gait(HPO:0002362)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Orphanet:313808)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Early-onset parkinsonism - intellectual deficit (Orphanet:2379)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency (Orphanet:352497)
L1 syndrome (Orphanet:275543)
MASA syndrome (Orphanet:2466)
PARKINSON DISEASE 20, EARLY-ONSET (OMIM:615530)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
X-linked complicated spastic paraplegia type 1 (Orphanet:306617)
X-linked spastic paraplegia type 16 (Orphanet:100997)
Young adult-onset Parkinsonism (Orphanet:2828)