FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term pontocerebellar hypoplasia type 16 ID (Ontology) DOID:0112333 (Human Disease)
Definition A pontocerebellar hypoplasia characterized by hypotonia and severe global developmental delay apparent from early infancy that has_material_basis_in homozygous or compound heterozygous mutation in the MINPP1 gene on chromosome 10q23.2.
Also Known As "PCH16"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 pontocerebellar hypoplasia type 16       2
 for disease ribbon | pontocerebellar hypoplasia type 16       2
 model of | pontocerebellar hypoplasia type 16       2
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
neurodegenerative disease        |
 |__pontocerebellar hypoplasia___|
                                 pontocerebellar hypoplasia type 16  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
pontocerebellar hypoplasia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "PCH16" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
MIM:619527