G2Cdb::Human Disease report

Disease id
D00000133
Name
May-Hegglin anomaly
Nervous system disease
no

Genes (1)

Gene Name/Description Mutations Found Literature Mutations Type Genetic association?
G00002004 MYH9
myosin, heavy chain 9, non-muscle
Y (16978745) Unknown (?) Y
G00002004 MYH9
myosin, heavy chain 9, non-muscle
Y (16642488) Unknown (?) Y

References

Literature (2)

Pubmed - human_disease

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EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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