Disease #00769 (FGS4 (FG syndrome, type 4 (FGS4)), OMIM:300422)

Official abbreviation FGS4
Name FG syndrome, type 4 (FGS4)
OMIM ID 300422
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CASK
Associated tissues -
Disease features -
Remarks -