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MED11

mediator complex subunit 11

HCNC Approved Symbol
MED11 (HGNC:32687)
Genomic Coordinates
17:4,731,428 - 4,733,607 (17p13.2)
Synonyms
HSPC296, MGC88387
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities
620327AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MED11 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results