conductive deafness-malformed external ear syndrome
MONDO:0009083Mondo
Findings
No curated finding names conductive deafness-malformed external ear 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.
- Conductive hearing impairmentHPOHP:0000405
- Very frequent (80% to 99% of cases)
- Low-set earsHPOHP:0000369
- Very frequent (80% to 99% of cases)
- MicrotiaHPOHP:0008551
- Very frequent (80% to 99% of cases)
- Abnormality of the middle ear ossiclesHPOHP:0004452
- Frequent (30% to 79% of cases)
- Global developmental delayHPOHP:0001263
- Frequent (30% to 79% of cases)
- High palateHPOHP:0000218
- Frequent (30% to 79% of cases)
- HypogonadismHPOHP:0000135
- Frequent (30% to 79% of cases)
- Overfolded helixHPOHP:0000396
- Frequent (30% to 79% of cases)
- Abnormal pinna morphologyHPOHP:0000377
- Occasional (5% to 29% of cases)
- Hernia of the abdominal wallHPOHP:0004299
- Occasional (5% to 29% of cases)
- Preauricular skin tagHPOHP:0000384
- Occasional (5% to 29% of cases)
- Sensorineural hearing impairmentHPOHP:0000407
- Occasional (5% to 29% of cases)
Show the remaining 1
- Stenosis of the external auditory canalHPOHP:0000402
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
2 names
Resolves to: conductive deafness-malformed external ear syndrome
- Also called
- conductive hearing loss-malformed external ear syndromeMengel-Konigsmark syndrome