Joubert syndrome 31
MONDO:0033310Mondo
Findings
No curated finding names Joubert syndrome 31 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
HPO, annotations 2026-09-02
Features
10 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.
- Global developmental delayHPOHP:0001263
- 4 of 4 reported patients
- HypotoniaHPOHP:0001252
- 4 of 4 reported patients
- Molar tooth sign on MRIHPOHP:0002419
- 4 of 4 reported patients
- Truncal ataxiaHPOHP:0002078
- 2 of 4 reported patients
- Duane anomalyHPOHP:0009921
- 1 of 4 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 1 of 4 reported patients
- NystagmusHPOHP:0000639
- 1 of 4 reported patients
- Oculomotor apraxiaHPOHP:0000657
- 1 of 4 reported patients
- StrabismusHPOHP:0000486
- 1 of 4 reported patients
- VentriculomegalyHPOHP:0002119
- 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.
- CEP120HGNC:26690
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
Where it sits
- A kind of