Disease #05045

Official abbreviation PCH-5
Name hypoplasia, pontocerebellar?, type 5 (PCH-5)
OMIM ID 610204
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TSEN54
Associated tissues -
Disease features -
Remarks -