Tyrosinemia type II

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What is tyrosinemia type II?

Tyrosinemia is a genetic disorder characterized by elevated blood levels of the amino acid tyrosine, a building block of most proteins. Type II tyrosinemia is caused by a deficiency of the enzyme tyrosine aminotransferase.

Common symptoms reported by people with tyrosinemia type II

Common symptoms
How bad it is
What people are taking for it

Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.
Last updated:

Treatments taken by people with tyrosinemia type II

No data

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Compare treatments taken by people with tyrosinemia type II

No data

Let’s build this page together! When you share what it’s like to have tyrosinemia type II through your profile, those stories and data appear here too.

Got a question about living with tyrosinemia type II? Members in the forum might have the answers.

Who has tyrosinemia type II on PatientsLikeMe?


Age
Age Proportion # of patients
<20 0
20s 0
30s 1
40s 0
50s 0
60s 0
70+ 0
Age at first symptom
Age at first symptom Proportion # of patients
0-19 years 0
20-29 years 0
30-39 years 0
40-49 years 0
50-59 years 0
60-69 years 0
70+ years 0

Sex

Distribution of sex

0% Female
100% Male

Diagnosis status
Diagnosis status Proportion # of patients
Diagnosed 0
Not Diagnosed 0

These charts show data from tyrosinemia type II patients who have completed their condition history
Last updated:
No data

Let’s build this page together! When you share what it’s like to have tyrosinemia type II through your profile, those stories and data appear here too.

Got a question about living with tyrosinemia type II? Members in the forum might have the answers.