Disease #03976

Official abbreviation -
Name Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige
OMIM ID 615508
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DSG1
Associated tissues -
Disease features -
Remarks -