polydactyly-myopia syndrome
Findings
No curated finding names polydactyly-myopia syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Polydactyly-myopia syndrome is an exceedingly rare autosomal dominant developmental anomaly reported in 1986 in nine individuals among four generations of the same family. The syndrome is characterized clinically by four-limb postaxial polydactyly and progressive myopia. There have been no further descriptions in the literature since 1986.
Definition from the Mondo Disease Ontology (MONDO:0008268), read 2026-09-29. CC BY 4.0.
Features
5 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.
- MyopiaHPOHP:0000545
- Very frequent (80% to 99% of cases)
- Postaxial hand polydactylyHPOHP:0001162
- Very frequent (80% to 99% of cases)
- CryptorchidismHPOHP:0000028
- Frequent (30% to 79% of cases)
- Femoral herniaHPOHP:0100541
- Frequent (30% to 79% of cases)
- Inguinal herniaHPOHP:0000023
- Frequent (30% to 79% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: polydactyly-myopia syndrome
- Also called
- Czeizel-Brooser syndrome