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Standards Ontologies Notations
MYH-9 related disease

Summary
Definition
A blood platelet disease that has_material_basis_in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.
Super Class
blood platelet disease
Disease Ontology
DOID:0060651
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4627 MYH9 myosin heavy chain 9
Displaying 1 entry
Gene ID Gene Symbol Description Source
17886 Myh9 myosin, heavy polypeptide 9, non-muscle
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024