Disease #00138 (autism (autism), OMIM:209850)

Official abbreviation autism
Name autism
OMIM ID 209850
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MAGEL2
Associated tissues -
Disease features -
Remarks -
Date created 2013-06-04 18:17:33 +02:00 (CEST)
Date last edited N/A