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Standards Ontologies Notations
autosomal dominant Alport syndrome

Summary
Definition
An Alport syndrome that has_material_basis_in heterozygous mutation in the COL4A3 gene.
Super Class
Alport syndrome autosomal dominant disease
Disease Ontology
DOID:0110032
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1285 COL4A3 collagen type IV alpha 3 chain
4627 MYH9 myosin heavy chain 9
Displaying all 2 entries
Gene ID Gene Symbol Description Source
12828 Col4a3 collagen, type IV, alpha 3
17886 Myh9 myosin, heavy polypeptide 9, non-muscle
Displaying 1 entry
Gene ID Gene Symbol Description Source
33727 Col4a1 Collagen type IV alpha 1
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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