HUPRA syndrome
human disease
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HUPRA syndrome
Summary
HUPRA syndrome is a developmental defect during embryogenesis[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- HUPRA syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- HUPRA syndrome's instance of is recorded as rare disease[4].
- HUPRA syndrome's instance of is recorded as class of disease[5].
- HUPRA syndrome is a type of mitochondrial disease[6].
- HUPRA syndrome is a type of genetic hypertension[7].
- HUPRA syndrome is a type of combined oxidative phosphorylation deficiency[8].
- HUPRA syndrome is a type of tubulopathy[9].
- HUPRA syndrome is a type of syndrome with pulmonary hypertension as a major feature[10].
- HUPRA syndrome is a type of rare genetic developmental defect during embryogenesis[11].
- HUPRA syndrome is a type of rare genetic respiratory disease[12].
- HUPRA syndrome is a type of inherited renal tubular disease[13].
- HUPRA syndrome's genetic association is recorded as SARS2[14].
Why It Matters
HUPRA syndrome is known by 6 alternative names across languages and contexts.[2]