Disease #00942 (COFS-1 (cerebrooculofacioskeletal syndrome, type 1 (COFS-1), OMIM:214150)

Official abbreviation COFS-1
Name cerebrooculofacioskeletal syndrome, type 1 (COFS-1
OMIM ID 214150
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ERCC6
Associated tissues -
Disease features -
Remarks -