Disease #00553 (FBCG-1 (fibrochondrogenesis, type 1 (FBCG-1)), OMIM:228520)

Official abbreviation FBCG-1
Name fibrochondrogenesis, type 1 (FBCG-1)
OMIM ID 228520
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene COL11A1
Associated tissues -
Disease features -
Remarks -