Disease #00650 (JWS (Jackson-Weiss syndrome), OMIM:123150)

Official abbreviation JWS
Name Jackson-Weiss syndrome
OMIM ID 123150
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes FGFR1, FGFR2
Associated tissues -
Disease features -
Remarks -