Disease #00986 (COFS-3 (cerebrooculofacioskeletal syndrome, type 3 (COFS-3))

Official abbreviation COFS-3
Name cerebrooculofacioskeletal syndrome, type 3 (COFS-3
OMIM ID -
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ERCC5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A