PKU vs. HCU

AccuGo ships as two separate apps in the App Store — AccuGo for PKU and AccuGo for HCU. They share the same code base and core feature set; what differs is which nutrient is the focus, which settings exist, and a few platform features.

Conditions, briefly

Phenylketonuria (PKU) is a genetic condition where the body can't break down the amino acid phenylalanine. The diet limits phenylalanine; protein and exchanges (10–50 mg of phenylalanine each, by convention) are common ways of expressing the daily allowance.

Homocystinuria (HCU) is a related but distinct condition affecting the body's processing of methionine. The diet limits methionine instead; protein is the most commonly tracked surrogate.

AccuGo doesn't make medical recommendations — it just records what you eat in the units your dietitian uses.

Feature differences

FeaturePKUHCU
Primary nutrient Phenylalanine (mg) Methionine (mg)
Default tracking mode Phenylalanine, Exchanges, Calories Protein, Calories
Exchanges Yes (default size 15 mg) Not available
Simplified diet option Yes Not available
Daily target notification Yes Not available
Background refresh Yes Not available
External resource link in More Not shown HCU Network Australia
Community filter Foods with phe or protein values Foods with met or protein values
Bundle identifier prefix com.accugo.pku com.accugo (hcu target)

What's the same

Can one person use both?

Technically yes — you can install both apps and sign in to the same account on each. But the tracking mode is a per-account setting that affects both, and the daily summary differs by app, so you'd be looking at the same data through two different lenses. In practice, families pick the variant that matches their condition and stick with it.