Disease #00113 (FFDD3 (dysplasia, dermal, focal facial, type 3 (FFDD-3, Setleis)), OMIM:227260)

Official abbreviation FFDD3
Name dysplasia, dermal, focal facial, type 3 (FFDD-3, Setleis)
OMIM ID 227260
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease 3
Associated with 1 gene TWIST2
Associated tissues -
Disease features -
Remarks -