peroxisome biogenesis disorder 1A (Zellweger)
MONDO:0008953Mondo
Findings
No curated finding names peroxisome biogenesis disorder 1A (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
- Congenital onset · Infantile onset · Neonatal onset · Death in childhood
HPO, annotations 2026-09-02
Features
49 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.
- Ankle clonusHPOHP:0011448
- 1 of 1 reported patient
- ApneaHPOHP:0002104
- 1 of 1 reported patient
- Aspiration pneumoniaHPOHP:0011951
- 1 of 1 reported patient
- Atrial septal defectHPOHP:0001631
- 1 of 1 reported patient
- Bilateral single transverse palmar creasesHPOHP:0007598
- 1 of 1 reported patient
- Cerebral cortical atrophyHPOHP:0002120
- 1 of 1 reported patient · Infantile onset
- Cleft palateHPOHP:0000175
- 1 of 1 reported patient
- Decreased muscle massHPOHP:0003199
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 1 reported patient
- Elevated circulating alanine aminotransferase concentrationHPOHP:0031964
- 2 of 2 reported patients
- Elevated circulating aspartate aminotransferase concentrationHPOHP:0031956
- 2 of 2 reported patients
Show the remaining 37
- Elevated circulating long chain fatty acid concentrationHPOHP:0003455
- 3 of 3 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 1 reported patient
- Fetal distressHPOHP:0025116
- 1 of 1 reported patient
- Focal clonic seizureHPOHP:0002266
- 1 of 1 reported patient
- Focal impaired awareness seizureHPOHP:0002384
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 4 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.
- PEX1HGNC:8850
- Definitive · Ambry Genetics · Autosomal recessive · 2017
- Definitive · Myriad Women's Health · Autosomal recessive · 2018