Search Ontology:
Human Disease

Tietz syndrome

Term ID
DOID:0090002
Synonyms
  • albinism-deafness of Tietz
  • hypopigmentation/deafness of Tietz
  • Tietz albinism-deafness syndrome
Definition
A syndrome that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair that has_material_basis_in mutation in the MITF gene on chromosome 3p13. (3)
References
Ontology
Human Disease   ( DOID:0090002 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.