hydrocephalus, congenital communicating, 1
MONDO:0032862Mondo
Findings
No curated finding names hydrocephalus, congenital communicating, 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
4 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.
- Communicating hydrocephalusHPOHP:0001334
- 3 of 3 reported patients · Antenatal onset
- Neurodevelopmental delayHPOHP:0012758
- 3 of 3 reported patients
- SeizureHPOHP:0001250
- 3 of 3 reported patients
- VentriculomegalyHPOHP:0002119
- 3 of 3 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.
- TRIM71HGNC:32669
- Strong · Ambry Genetics · Autosomal dominant · 2024
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2019
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · G2P · Autosomal dominant · 2026
- Limited · Ambry Genetics · Autosomal dominant · 2018
Where it sits
- A kind of