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Term ID: | 8230 |
Name: | Olivopontocerebellar hypoplasia, fetal-onset |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D009849 |
TreeNumbers: | C10.228.140.079.612.600/C537745 |C10.228.140.252.700.650/C537745 |C10.228.662.550.600/C537745 |C10.228.854.787.750/C537745 |C10.574.500.825.650/C537745 |C10.574.625.600/C537745 |C10.574.750/C537745 |C16.320.400.780.750/C537745 |
Synonyms: | Pontocerebellar hypoplasia, type 5 |Pontocerebellar Hypoplasia Type 5 |
Slim Mappings: | Genetic disease (inborn)|Nervous system disease |
Reference: |
MedGen: C537745
MeSH: C537745
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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