Disease #00749

Official abbreviation COFS-2
Name cerebrooculofacioskeletal syndrome, type 2 (COFS-2
OMIM ID 610756
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ERCC2
Associated tissues -
Disease features -
Remarks -