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 91 - 100 of 100 in total
Gene ID Gene Symbol Description Source
57016 AKR1B10 aldo-keto reductase family 1 member B10
57104 PNPLA2 patatin like phospholipase domain containing 2
57126 CD177 CD177 molecule
57214 CEMIP cell migration inducing hyaluronidase 1
64083 GOLPH3 golgi phosphoprotein 3
64781 CERK ceramide kinase
79679 VTCN1 V-set domain containing T cell activation inhibitor 1
113026 PLCD3 phospholipase C delta 3
130120 REG3G regenerating family member 3 gamma
347527 ARSH arylsulfatase family member H

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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