Disease #03443

Official abbreviation PCH-2D
Name hypoplasia, pontocerebellar, type 2D (PCH-2D)
OMIM ID 613811
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SEPSECS
Associated tissues -
Disease features -
Remarks -