Perrault syndrome 6
MONDO:0033047Mondo
Findings
No curated finding names Perrault syndrome 6 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
7 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Hypoplasia of the uterusHPOHP:0000013
- 1 of 1 reported patient
- Sensorineural hearing impairmentHPOHP:0000407
- 2 of 2 reported patients
- Streak ovaryHPOHP:0010464
- 1 of 1 reported patient
- Primary amenorrheaHPOHP:0000786
- 1 of 2 reported patients · Female
- Secondary amenorrheaHPOHP:0000869
- 1 of 2 reported patients · Female
- Irregular menstruationHPOHP:0000858
- Premature ovarian insufficiencyHPOHP:0008209
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ERAL1HGNC:3424
- Moderate · PanelApp Australia · Autosomal recessive · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2018
Where it sits
- A kind of