auriculocondylar syndrome 4
MONDO:0957543Mondo
Findings
No curated finding names auriculocondylar syndrome 4 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
HPO, annotations 2026-09-02
Features
11 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.
- Hearing impairmentHPOHP:0000365
- 6 of 6 reported patients
- Full cheeksHPOHP:0000293
- 8 of 10 reported patients
- Narrow mouthHPOHP:0000160
- 8 of 10 reported patients
- Question mark earHPOHP:0030022
- 8 of 10 reported patients
- Facial asymmetryHPOHP:0000324
- 6 of 10 reported patients
- MicrognathiaHPOHP:0000347
- 6 of 10 reported patients
- GlossoptosisHPOHP:0000162
- 4 of 9 reported patients
- ApneaHPOHP:0002104
- 4 of 10 reported patients
- Postauricular skin tagHPOHP:0004451
- 2 of 10 reported patients
- Cleft palateHPOHP:0000175
- 1 of 10 reported patients
- Global developmental delayHPOHP:0001263
- 0 of 10 reported patients
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.
- HDAC9HGNC:14065
- Limited · Ambry Genetics · Autosomal dominant · 2024
Where it sits
- A kind of