Poor coordination
Symptom Information:
Symptom ID: | HPO:0002370 | ||
Synonyms: |
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Quality: | |||
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 central motor function(HPO:0011442) Abnormality of coordination(HPO:0011443) Incoordination(HPO:0002311) Poor coordination(HPO:0002370) MedDRA: |
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Database Frequency: | 15 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION | (OMIM:270500) |
Alström syndrome | (Orphanet:64) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Methylcobalamin deficiency type cblG | (Orphanet:2170) |
Moebius syndrome | (Orphanet:570) |
Monosomy 18q | (Orphanet:1600) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SOTOS SYNDROME 1 | (OMIM:117550) |
Sotos syndrome | (Orphanet:821) |
Williams syndrome | (Orphanet:904) |
XFE PROGEROID SYNDROME | (OMIM:610965) |