hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
MONDO:0019073Mondo
Findings
No curated finding names hypotrichosis-lymphedema-telangiectasia-renal defect syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset · Fetal onset
HPO, annotations 2026-09-02
Features
5 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.
- Hydrocele testisHPOHP:0000034
- 2 of 2 reported patients
- LymphedemaHPOHP:0001004
- 5 of 5 reported patients
- Sparse scalp hairHPOHP:0002209
- 4 of 4 reported patients
- Dermal translucencyHPOHP:0010648
- 2 of 4 reported patients
- Nonimmune hydrops fetalisHPOHP:0001790
- 1 of 5 reported patients · Fetal onset
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.
- SOX18HGNC:11194
- Strong · Genomics England PanelApp · Autosomal dominant · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2024