|  Help  |  About  |  Contact Us

DO Term : tyrosinemia type II [DOID:0050725] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A tyrosinemia that has_material_basis_in deficiency of hepatic tyrosine aminotransferase located_in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels.
  • synonyms:
  • Oculocutaneous tyrosinemia,
  • 276600,
  • OMIM:276600,
  • Richner-Hanhart syndrome
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents