Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire coronal suture of skull |
Is a |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
|
Acrocephaly |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Acrocephaly |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Fibroblast growth factor receptor 3-related craniosynostosis (disorder) |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Acrocephaly |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Brachycephaly |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
3 |
Bicoronal craniosynostosis |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
3 |
Brachycephaly |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
4 |
Acrocephaly |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
3 |
Spheno-fronto-parietal craniofaciosynostosis |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Spheno-fronto-parietal craniofaciosynostosis |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
5 |
Cloverleaf skull syndrome (disorder) |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Antley-Bixler syndrome |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
7 |
Unicoronal craniosynostosis |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
An abnormally high skull with shortness of anterior-posterior dimension. A type of craniosynostosis in which there is premature closure of the coronal suture resulting in an abnormally short anteroposterior diameter of the cranium. |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Bicoronal craniosynostosis |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
7 |
Craniosynostosis fibular aplasia syndrome (disorder) |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
2 |
Craniosynostosis fibular aplasia syndrome (disorder) |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Antley-Bixler syndrome |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
A syndromic craniosynostosis with a wide range of clinical findings even within a single family. Most have coronal synostosis however synostosis of other sutures, all sutures, macrocephaly without craniosynostosis, or a normal skull may be observed. Bilateral coronal synostosis usually results in brachycephaly with temporal bossing and facial symmetry. Craniofacial findings include widely spaced eyes, ptosis or proptosis, strabismus, and high arched palate or cleft lip/palate. Over 70% of patients have some form of hearing loss. Additional extracranial manifestations include otitis media, brachydactyly, broad toes, broad thumbs, clinodactyly, developmental delay and intellectual disability. Caused by mutation in the FGFR3 gene (4p16.3), encoding fibroblast growth factor receptor 3, which is required for normal skeleton development. Inheritance is autosomal dominant. |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
Cloverleaf skull, asphyxiating thoracic dysplasia syndrome (disorder) |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
2 |
Antley-Bixler syndrome |
Finding site |
False |
Structure of coronal suture of skull |
Inferred relationship |
Some |
3 |
Saethre-Chotzen syndrome |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
1 |
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
5 |
Cloverleaf skull, asphyxiating thoracic dysplasia syndrome (disorder) |
Finding site |
True |
Structure of coronal suture of skull |
Inferred relationship |
Some |
4 |