Disease #01051 (PCWH (syndrome, PCWH (PCWH)), OMIM:609136)

Official abbreviation PCWH
Name syndrome, PCWH (PCWH)
OMIM ID 609136
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SOX10
Associated tissues -
Disease features -
Remarks -