Search Ontology:
Human Disease

pontocerebellar hypoplasia type 2

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