Leber congenital amaurosis with early-onset deafness
MONDO:0060650Mondo
Findings
No curated finding names Leber congenital amaurosis with early-onset deafness 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
- Congenital onset · Childhood onset
HPO, annotations 2026-09-02
Features
9 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.
- High hypermetropiaHPOHP:0008499
- 6 of 6 reported patients
- Reduced visual acuityHPOHP:0007663
- 6 of 6 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 6 of 6 reported patients · Juvenile onset
- NystagmusHPOHP:0000639
- 2 of 6 reported patients
- PhotophobiaHPOHP:0000613
- 2 of 6 reported patients
- Retinal pigment epithelial mottlingHPOHP:0007814
- 2 of 6 reported patients
- Peripapillary atrophyHPOHP:0500087
- 1 of 6 reported patients
- Hearing impairmentMondoHP:0000365
- Retinal degenerationHPOHP:0000546
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.
- TUBB4BHGNC:20771
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021