mental retardation, autosomal recessive 15 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills. (Human Disease Ontology, DOID_1059)
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1 genes associated with the mental retardation, autosomal recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MAN1B1 mannosidase, alpha, class 1B, member 1