Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire sagittal suture of skull |
Is a |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
|
Skafocefali |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Skafocefali |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Interparietal craniosynostosis (disorder) |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Interparietal craniosynostosis (disorder) |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
2 |
Cloverleaf skull syndrome (disorder) |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
5 |
A rare, multiple congenital anomalies syndrome with intellectual disability commonly characterized by facial dysmorphism (e.g. sagittal craniosynostosis, hypertelorism, strabismus, low-set dysplastic ears, retrognathia or micrognathia, mandibular ankyloses, cleft palate, aplasia uvulae), congenital heart defects (e.g. atrioventricular septal defect, anomalous venous return), genital anomalies (e.g. cryptorchidism, microphallus), as well as growth delay and intellectual disability. In some cases, tracheobronchial anomalies, large joint contractures, syndactyly, rib anomalies and hypoplastic kidneys are reported. Rarely, no cardiac anomaly may be reported. |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
2 |
A rare syndromic craniosynostosis characterized by sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism. |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
7 |
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
9 |
Skafocefali |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
3 |
Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
3 |
A rare, multiple congenital anomalies syndrome with intellectual disability commonly characterized by facial dysmorphism (e.g. sagittal craniosynostosis, hypertelorism, strabismus, low-set dysplastic ears, retrognathia or micrognathia, mandibular ankyloses, cleft palate, aplasia uvulae), congenital heart defects (e.g. atrioventricular septal defect, anomalous venous return), genital anomalies (e.g. cryptorchidism, microphallus), as well as growth delay and intellectual disability. In some cases, tracheobronchial anomalies, large joint contractures, syndactyly, rib anomalies and hypoplastic kidneys are reported. Rarely, no cardiac anomaly may be reported. |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Cloverleaf skull syndrome (disorder) |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
3 |
This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies. |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
4 |
Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
A rare syndromic craniosynostosis characterized by sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism. |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
4 |
Cloverleaf skull, asphyxiating thoracic dysplasia syndrome (disorder) |
Finding site |
False |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
4 |
Finding of sagittal suture palpable vaginally |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Sagittal suture in anteroposterior diameter |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Sagittal suture in transverse diameter |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Sagittal suture in oblique diameter |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Sagittal suture in right oblique diameter |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
1 |
Sagittal suture in left oblique diameter |
Finding site |
True |
Structure of sagittal 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 sagittal suture of skull |
Inferred relationship |
Some |
5 |
Cloverleaf skull, asphyxiating thoracic dysplasia syndrome (disorder) |
Finding site |
True |
Structure of sagittal suture of skull |
Inferred relationship |
Some |
3 |