craniosynostosis-scoliosis syndrome
MONDO:0980974Mondo
Findings
No curated finding names craniosynostosis-scoliosis syndrome 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
78 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 facial shapeHPOHP:0001999
- 1 of 1 reported patient
- Anal fistulaHPOHP:0010447
- 1 of 1 reported patient
- Anterior plagiocephalyHPOHP:0011326
- 1 of 1 reported patient
- Bilateral conductive hearing impairmentHPOHP:0008513
- 2 of 2 reported patients
- Bilateral cryptorchidismHPOHP:0008689
- 1 of 1 reported patient
- BrachycephalyHPOHP:0000248
- 2 of 2 reported patients
- Broad neckHPOHP:0000475
- 1 of 1 reported patient
- Caesarean sectionHPOHP:0011410
- 2 of 2 reported patients
- CraniosynostosisHPOHP:0001363
- 1 of 1 reported patient
- Delayed ability to walkHPOHP:0031936
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Dental malocclusionHPOHP:0000689
- 1 of 1 reported patient
Show the remaining 66
- Downslanted palpebral fissuresHPOHP:0000494
- 1 of 1 reported patient
- ExodeviationHPOHP:0020049
- 1 of 1 reported patient
- Facial asymmetryHPOHP:0000324
- 1 of 1 reported patient
- Failure to thriveHPOHP:0001508
- 1 of 1 reported patient
- Feeding difficultiesHPOHP:0011968
- 1 of 1 reported patient
- Glue earHPOHP:0040262
- 1 of 1 reported patient
Where it sits
- A kind of