Disease #00238 (GPHYSD2 (dysplasia, geleophysic, type 2 (GPHYSD-2)), OMIM:614185)

Official abbreviation GPHYSD2
Name dysplasia, geleophysic, type 2 (GPHYSD-2)
OMIM ID 614185
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 FBN1
Associated tissues -
Disease features -
Remarks -