Disease #05951 (COFG (cerebellar, ocular, craniofacial, and genital syndrome (COFG)), OMIM:618479)

Official abbreviation COFG
Name cerebellar, ocular, craniofacial, and genital syndrome (COFG)
OMIM ID 618479
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MAB21L1
Associated tissues -
Disease features -
Remarks -