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)
OTHER pontocerebellar hypoplasia type 2 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None