Broad-based gait
Symptom Information:
Symptom ID: | HPO:0002136 | |||||||
Synonyms: |
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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) Broad-based gait(HPO:0002136) MedDRA: |
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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) |