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Tyrosinemia type 2

ORPHA:28378DiseaseAutosomal recessiveAdolescent, Childhood, Infancy, Neonatal

Ассоциированные гены (1)

TAT
tyrosine aminotransferase
Disease-causing germline mutation(s) (loss of function) in
OMIM: 613018

Фенотипы (17)

Очень частый (80–99%)4
HP:0000962Hyperkeratosis
HP:0000982Palmoplantar keratoderma
HP:0001249Intellectual disability
HP:0007957Corneal opacity
Частый (30–79%)5
HP:0000613Photophobia
HP:0000639Nystagmus
HP:0000708Atypical behavior
HP:0000975Hyperhidrosis
HP:0004337Abnormality of amino acid metabolism
Периодический (5–29%)8
HP:0000252Microcephaly
HP:0000272Malar flattening
HP:0000572Visual loss
HP:0001250Seizure
HP:0001251Ataxia
HP:0001337Tremor
HP:0001597Abnormality of the nail
HP:0002167Abnormality of speech or vocalization

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы