OBO ID: DOID:0112328
Term Name: pontocerebellar hypoplasia type 2 Search Ontology:
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:
OTHER pontocerebellar hypoplasia type 2 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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