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Term ID: | 9123 |
Name: | Pontocerebellar Hypoplasia Type 2 |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D009849 |
TreeNumbers: | C10.228.140.079.612.600/C548070 |C10.228.140.252.700.650/C548070 |C10.228.662.550.600/C548070 |C10.228.854.787.750/C548070 |C10.574.500.825.650/C548070 |C10.574.625.600/C548070 |C10.574.750/C548070 |C16.320.400.780.750/C548070 |
Synonyms: | |
Slim Mappings: | Genetic disease (inborn)|Nervous system disease |
Reference: |
MedGen: C548070
MeSH: C548070
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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