Search Ontology:
Human Disease
pontocerebellar hypoplasia type 2
- Term ID
- DOID:0112328
- Synonyms
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- PCH2
- Definition
- A pontocerebellar hypoplasia characterized by pontocerebellar hypoplasia and progressive neocortical atrophy. https://medlineplus.gov/genetics/condition/pontocerebellar-hypoplasia/
- References
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- GARD:10705
- MESH:C548070
- ORDO:2524
- Ontology
- Human Disease ( DOID:0112328 )
- is a type of
-
- has subtype
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Genes Involved
Zebrafish Models