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Standards Ontologies Notations
pulmonary venoocclusive disease 1

Summary
Definition
A pulmonary venoocclusive disease that has_material_basis_in heterozygous mutation in the BMPR2 gene on chromosome 2q33.
Super Class
autosomal dominant disease pulmonary venoocclusive disease
Disease Ontology
DOID:0081268
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
659 BMPR2 bone morphogenetic protein receptor type 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
12168 Bmpr2 bone morphogenetic protein receptor type 2
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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