otoonychoperoneal syndrome
MONDO:0009822Mondo
Findings
No curated finding names otoonychoperoneal syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
13 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.
- Abnormal antihelix morphologyHPOHP:0009738
- Very frequent (80% to 99% of cases)
- Abnormal diaphysis morphologyHPOHP:0000940
- Very frequent (80% to 99% of cases)
- Abnormal helix morphologyHPOHP:0011039
- Very frequent (80% to 99% of cases)
- Abnormal nail morphologyHPOHP:0001597
- Very frequent (80% to 99% of cases)
- Aplasia/Hypoplasia of the earlobesHPOHP:0009906
- Very frequent (80% to 99% of cases)
- Flexion contractureHPOHP:0001371
- Very frequent (80% to 99% of cases)
- Knee flexion contractureHPOHP:0006380
- Very frequent (80% to 99% of cases)
- MacrotiaHPOHP:0000400
- Very frequent (80% to 99% of cases)
- Mild intellectual disabilityHPOHP:0001256
- Very frequent (80% to 99% of cases)
- Popliteal pterygiumHPOHP:0009756
- Very frequent (80% to 99% of cases)
- Underfolded helixHPOHP:0008577
- Very frequent (80% to 99% of cases)
- DolichocephalyHPOHP:0000268
- Frequent (30% to 79% of cases)
Show the remaining 1
- Upslanted palpebral fissureHPOHP:0000582
- Frequent (30% to 79% of cases)