obsolete Matthew-Wood syndrome

Summary
Definition
A syndrome that is characterized by microphthalmia or anophthalmia, pulmonary agenesis, and diaphragmatic defect.
External Links
Disease Ontology
DOID:0050819
Related Genes
Displaying entries 21 - 30 of 100 in total
Gene ID Gene Symbol Description Source
2215 FCGR3B Fc gamma receptor IIIb
2220 FCN2 ficolin 2
2224 FDPS farnesyl diphosphate synthase
2262 GPC5 glypican 5
2525 FUT3 fucosyltransferase 3 (Lewis blood group)
2526 FUT4 fucosyltransferase 4
2571 GAD1 glutamate decarboxylase 1
2591 GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
2597 GAPDH glyceraldehyde-3-phosphate dehydrogenase
2752 GLUL glutamate-ammonia ligase

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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