Disease Browser
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Parent Node: Cerebellar Ataxia (D002524) | Parent Node: Deafness (D003638) | Parent Node: Myoclonus (D009207) | ..Starting node ..Myoclonus, Cerebellar Ataxia, and Deafness (C563549)
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Sister Nodes: | ..Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia (C566188)
| ..Convulsive Disorder, Familial, with Prenatal or Early Onset (C565678)
| ..EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE (OMIM:254900)
| ..Feigenbaum Bergeron Richardson syndrome (C536178)
| ..Herrmann syndrome (C538113)
| ..Jankovic Rivera syndrome (C537563)
| ..Myoclonus, Cerebellar Ataxia, and Deafness (C563549)
| ..Nystagmus, Myoclonic (C564088)
| ..Opsoclonus-Myoclonus Syndrome (D053578) 1
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 7644 |
Name: | Myoclonus, Cerebellar Ataxia, and Deafness |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002524|MESH:D003638|MESH:D009207 |
TreeNumbers: | C09.218.458.341.186/C563549 |C10.228.140.252.190/C563549 |C10.597.350.090.500/C563549 |C10.597.350.500/C563549 |C10.597.751.418.341.186/C563549 |C23.888.592.350.090.200/C563549 |C23.888.592.350.500/C563549 |C23.888.592.763.393.341.186/C563549 |
Synonyms: | |
Slim Mappings: | Ear-nose-throat disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C563549
MeSH: C563549
OMIM: 159800;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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