familial congenital nasolacrimal duct obstruction
MONDO:0007871Mondo
Findings
No curated finding names familial congenital nasolacrimal duct obstruction yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
2 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.
- EpiphoraHPOHP:0009926
- 4 of 4 reported patients
- DacryocystoceleHPOHP:0030752
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.
- IGSF3HGNC:5950
- Supportive · Orphanet · Autosomal recessive · 2021
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2018