Disease #00627 (CRS-1 (craniosynostosis, type 1 (CRS-1)), OMIM:123100)

Official abbreviation CRS-1
Name craniosynostosis, type 1 (CRS-1)
OMIM ID 123100
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TWIST1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A