Disease #00820 (mental retardation, X-linked, Snyder-Robinson type, OMIM:309583)

Official abbreviation -
Name mental retardation, X-linked, Snyder-Robinson type
OMIM ID 309583
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SMS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A