Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C564570
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Genes

2 genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
AMMECR1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 2.88009
AMMEC Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis 2.88009