Broad-based gait

Symptom Information:

Symptom ID: HPO:0002136
Synonyms:
Broad based gait [HPO:0002136]
Wide based gait [HPO:0002136]
Wide-based gait [HPO:0002136]
Broad-based gait [OMIM:Broad-based gait]
Wide-based gait [OMIM:Wide-based gait]
Broad-based gait (1 patient) [OMIM:Broad-based gait (1 patient)]
Gait wide-based [OMIM:Gait wide-based]
Quality:
Cross references:
OMIM: "Broad-based gait" [OMIM:Broad-based gait]
OMIM: "Wide-based gait" [OMIM:Wide-based gait]
OMIM: "Broad-based gait (1 patient)" [OMIM:Broad-based gait (1 patient)]
OMIM: "Gait wide-based" [OMIM:Gait wide-based]
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)
                   Broad-based gait(HPO:0002136)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

2q32q33 microdeletion syndrome (Orphanet:251019)
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT (OMIM:206570)
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION (OMIM:270500)
Angelman syndrome (Orphanet:72)
Bilateral frontoparietal polymicrogyria (Orphanet:101070)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 (OMIM:224050)
CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE (OMIM:605388)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R (OMIM:615490)
Cerebellar ataxia, Cayman type (Orphanet:94122)
Distal monosomy 10q (Orphanet:96148)
Dysequilibrium syndrome (Orphanet:1766)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY,AND SHORT STATURE (OMIM:609037)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 (OMIM:616158)
Monosomy 18q (Orphanet:1600)
Monosomy 22q13 (Orphanet:48652)
NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX (OMIM:162370)
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE (OMIM:258650)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Posterior column ataxia - retinitis pigmentosa (Orphanet:88628)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SPINOCEREBELLAR ATAXIA 40 (OMIM:616053)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
Spheroid body myopathy (Orphanet:268129)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Spinocerebellar ataxia type 29 (Orphanet:208513)
USHER SYNDROME, TYPE IIIB (OMIM:614504)
Wiedemann-Steiner syndrome (Orphanet:319182)
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome (Orphanet:85295)
Zunich-Kaye syndrome (Orphanet:3474)