chondrodysplasia-pseudohermaphroditism syndrome

Summary
Synonym
  • Nivelon-Nivelon-Mabille syndrome
  • chondrodysplasia-disorder of sex development syndrome
Definition
A syndrome characterized by the clinical features of 46,XY complete gonadal dysgenesis in association with severe dwarfism with generalized chondrodysplasia.
Super Class
syndrome
External Links
Disease Ontology
DOID:0060644
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 35 in total
Gene ID Gene Symbol Description Source
1634 DCN decorin
2348 FOLR1 folate receptor alpha
2597 GAPDH glyceraldehyde-3-phosphate dehydrogenase
2653 GCSH glycine cleavage system protein H
2720 GLB1 galactosidase beta 1
2731 GLDC glycine decarboxylase
2821 GPI glucose-6-phosphate isomerase
3339 HSPG2 heparan sulfate proteoglycan 2
4968 OGG1 8-oxoguanine DNA glycosylase
5224 PGAM2 phosphoglycerate mutase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
852796 GUP1 O-acyltransferase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024