Disease #03892 (SYM1B (symphalangism, proximal, type 1B (SYM1B)), OMIM:615298)

Official abbreviation SYM1B
Name symphalangism, proximal, type 1B (SYM1B)
OMIM ID 615298
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 GDF5
Associated tissues -
Disease features -
Remarks -