peroxisome biogenesis disorder 5A (Zellweger)
MONDO:0013932Mondo
Findings
No curated finding names peroxisome biogenesis disorder 5A (Zellweger) yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Death in infancy · Congenital onset · Neonatal onset · Death in adolescence · Childhood onset
HPO, annotations 2026-09-02
Features
47 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.
- HypotoniaHPOHP:0001252
- 3 of 4 reported patients
- Increased circulating very long-chain fatty acid concentrationHPOHP:0033643
- 3 of 4 reported patients
- AreflexiaHPOHP:0001284
- 2 of 4 reported patients
- Elevated circulating alanine aminotransferase concentrationHPOHP:0031964
- 2 of 4 reported patients
- Elevated circulating aspartate aminotransferase concentrationHPOHP:0031956
- 2 of 4 reported patients
- HepatomegalyHPOHP:0002240
- 2 of 4 reported patients
- SeizureHPOHP:0001250
- 2 of 4 reported patients
- Tricuspid regurgitationHPOHP:0005180
- 2 of 4 reported patients
- Wide anterior fontanelHPOHP:0000260
- 2 of 4 reported patients
- CryptorchidismHPOHP:0000028
- 1 of 3 reported patients · Male
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 4 reported patients
- Aortic regurgitationHPOHP:0001659
- 1 of 4 reported patients
Show the remaining 35
- AthetosisHPOHP:0002305
- 1 of 4 reported patients
- Atrial septal defectHPOHP:0001631
- 1 of 4 reported patients
- CataractHPOHP:0000518
- 1 of 4 reported patients
- Cerebellar atrophyHPOHP:0001272
- 1 of 4 reported patients
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 4 reported patients
- Cerebellar vermis atrophyHPOHP:0006855
- 1 of 4 reported patients
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.
- PEX2HGNC:9717
- Definitive · Myriad Women's Health · Autosomal recessive · 2018
- Definitive · G2P · Autosomal recessive · 2017