Tietz syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Tietz syndrome is a genetic hypopigmentation and deafness syndrome characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair. (Orphanet Rare Disease Ontology, Orphanet_42665)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536919
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Genes

1 genes/proteins associated with the disease Tietz syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MITF microphthalmia-associated transcription factor 2.88009