hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
MONDO:0060666Mondo
Findings
No curated finding names hypotonia, ataxia, developmental delay, and tooth enamel 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
HPO, annotations 2026-09-02
Features
17 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.
- AtaxiaHPOHP:0001251
- 4 of 4 reported patients
- Enamel hypoplasiaHPOHP:0006297
- 4 of 4 reported patients
- Gait ataxiaHPOHP:0002066
- 3 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 4 of 4 reported patients
- HypotoniaHPOHP:0001252
- 4 of 4 reported patients
- Motor delayHPOHP:0001270
- 4 of 4 reported patients
- Delayed ability to sitHPOHP:0025336
- 3 of 4 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 3 of 4 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 4 reported patients
- Intellectual disabilityHPOHP:0001249
- 3 of 4 reported patients
- Cerebellar atrophyHPOHP:0001272
- 2 of 4 reported patients
- Inability to walkHPOHP:0002540
- 2 of 4 reported patients
Show the remaining 5
- Increased variability in muscle fiber diameterHPOHP:0003557
- 2 of 4 reported patients
- Deeply set eyeHPOHP:0000490
- 1 of 4 reported patients
- Frontal bossingHPOHP:0002007
- 1 of 4 reported patients
- High palateHPOHP:0000218
- 1 of 4 reported patients
- RetrognathiaHPOHP:0000278
- 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.
- CTBP1HGNC:2494
- Strong · Illumina · Autosomal dominant · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · G2P · Autosomal dominant · 2025
- Strong · Broad Center for Mendelian Genomics · Autosomal dominant · 2024
Where it sits
- A kind of