Disease #01110 (MRD-3 (mental retardation, autosomal dominant, type 3 (MRD-3)), OMIM:612580)

Official abbreviation MRD-3
Name mental retardation, autosomal dominant, type 3 (MRD-3)
OMIM ID 612580
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CDH15
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A