Bimanual synkinesia
Symptom Information:
Symptom ID: | HPO:0001335 | |||||
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) Bimanual synkinesia(HPO:0001335) MedDRA: |
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Database Frequency: | 9 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Familial congenital mirror movements | (Orphanet:238722) |
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA | (OMIM:308700) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA | (OMIM:308750) |
MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:604321) |
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:614852) |
MIRROR MOVEMENTS 2 | (OMIM:614508) |
MIRROR MOVEMENTS 3 | (OMIM:616059) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |