Disease #01725 (CSTLO (Costello syndrome (CSTLO)), OMIM:218040)

Official abbreviation CSTLO
Name Costello syndrome (CSTLO)
OMIM ID 218040
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene HRAS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A