Ornithine aminotransferase deficiency (Q7103623)

From Wikidata
Jump to: navigation, search
Human disease
  • gyrate atrophy
  • Gyrate atrophy of the choroid and/or retina
  • Ornithinemia with gyrate atrophy (disorder)
  • gyrate atrophy of the retina
  • Ornithinemia with gyrate atrophy
edit
Language Label Description Also known as
English
Ornithine aminotransferase deficiency
Human disease
  • gyrate atrophy
  • Gyrate atrophy of the choroid and/or retina
  • Ornithinemia with gyrate atrophy (disorder)
  • gyrate atrophy of the retina
  • Ornithinemia with gyrate atrophy

Statements

Identifiers

 
edit
edit
    edit
      edit
        edit
          edit
            edit
              edit