Myxedema Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11634)
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Genes

3 genes associated with the Myxedema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
C4A complement component 4A (Rodgers blood group)
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
CTLA4 cytotoxic T-lymphocyte-associated protein 4