pseudo-TORCH syndrome 2
MONDO:0018828Mondo
Findings
No curated finding names pseudo-TORCH syndrome 2 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
- Neonatal onset · Fetal onset
HPO, annotations 2026-09-02
Features
24 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.
- Acute respiratory distress syndromeHPOHP:0033677
- 1 of 1 reported patient
- Fetal distressHPOHP:0025116
- 1 of 1 reported patient
- Lateral ventricle dilatationHPOHP:0006956
- 1 of 1 reported patient
- Respiratory insufficiencyHPOHP:0002093
- 4 of 4 reported patients
- Cerebral hemorrhageHPOHP:0001342
- 5 of 6 reported patients
- SeizureHPOHP:0001250
- 4 of 5 reported patients
- PetechiaeHPOHP:0000967
- 3 of 5 reported patients
- ThrombocytopeniaHPOHP:0001873
- 3 of 5 reported patients
- Patent ductus arteriosusHPOHP:0001643
- 2 of 5 reported patients
- Abnormal renal corticomedullary differentiationHPOHP:0005932
- 1 of 5 reported patients
- AscitesHPOHP:0001541
- 1 of 5 reported patients
- BradycardiaHPOHP:0001662
- 1 of 5 reported patients
Show the remaining 12
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 5 reported patients
- Cerebral calcificationHPOHP:0002514
- 1 of 5 reported patients
- Elevated circulating hepatic transaminase concentrationHPOHP:0002910
- 1 of 5 reported patients
- HepatomegalyHPOHP:0002240
- 1 of 5 reported patients
- Lactic acidosisHPOHP:0003128
- 1 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 1 of 5 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.
- USP18HGNC:12616
- Definitive · Illumina · Autosomal recessive · 2022
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal recessive · 2016
- Moderate · Ambry Genetics · Autosomal recessive · 2022
- Supportive · Orphanet · Autosomal recessive · 2021