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Term ID: | 1631 |
Name: | CAPOS syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002524|MESH:D005532|MESH:D006319|MESH:D009896|MESH:D012021 |
TreeNumbers: | C05.330.495/C535351 |C05.660.585.512.380/C535351 |C09.218.458.341.887/C535351 |C10.228.140.252.190/C535351 |C10.292.700.225/C535351 |C10.597.350.090.500/C535351 |C10.597.704/C535351 |C10.597.751.418.341.887/C535351 |C11.640.451/C535351 |C16.131.621.585.380/C53535 |
Synonyms: | CAPOS |Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorineural hearing loss |Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, And Sensorineural Hearing Loss |Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hea |
Slim Mappings: | Congenital abnormality|Ear-nose-throat disease|Eye disease|Musculoskeletal disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C535351
MeSH: C535351
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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