Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire frontal suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Structure of frontozygomatic suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Structure of frontolacrimal suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Structure of frontomaxillary suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Structure of sphenofrontal suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Structure of frontonasal suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Structure of frontoethmoidal suture of skull |
Is a |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
|
Trigonocephaly |
Finding site |
False |
Structure of frontal suture of skull |
Inferred relationship |
Some |
1 |
Trigonocephaly |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
C syndrome is a rare multiple congenital anomaly/intellectual disability syndrome characterized by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability. |
Finding site |
False |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait. |
Finding site |
False |
Structure of frontal suture of skull |
Inferred relationship |
Some |
9 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991. |
Finding site |
False |
Structure of frontal suture of skull |
Inferred relationship |
Some |
7 |
A rare developmental defect during embryogenesis characterized by premature closure of metopic sutures and/or other sutures, short stature, and developmental delay. Dysmorphic features include trigonocephaly, metopic ridge, narrow forehead, bitemporal narrowing, arched eyebrows, hypotelorism, deep-set eyes, epicanthal folds, strabismus, wide nasal bridge, small pointed nose, anteverted nostrils, long philtrum, low-set ears, malar flattening, narrow mouth, thin lips, high-arched palate, crowded teeth, and micrognathia. Variable additional manifestations may include conductive hearing loss, cerebral (mainly involving the white matter), skeletal (e.g. brachymesophalangy of the fifth fingers), cardiovascular and renal anomalies, inguinal hernia, hypospadias, and seizures. |
Finding site |
False |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
C syndrome is a rare multiple congenital anomaly/intellectual disability syndrome characterized by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
1 |
A rare developmental defect during embryogenesis characterized by premature closure of metopic sutures and/or other sutures, short stature, and developmental delay. Dysmorphic features include trigonocephaly, metopic ridge, narrow forehead, bitemporal narrowing, arched eyebrows, hypotelorism, deep-set eyes, epicanthal folds, strabismus, wide nasal bridge, small pointed nose, anteverted nostrils, long philtrum, low-set ears, malar flattening, narrow mouth, thin lips, high-arched palate, crowded teeth, and micrognathia. Variable additional manifestations may include conductive hearing loss, cerebral (mainly involving the white matter), skeletal (e.g. brachymesophalangy of the fifth fingers), cardiovascular and renal anomalies, inguinal hernia, hypospadias, and seizures. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
1 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
Interfrontal craniofaciosynostosis |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
Isolated trigonocephaly is a nonsyndromic form of craniosynostosis characterised by the premature fusion of the metopic suture. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the metopic and sagittal sutures, resulting in trigonocephaly and scaphocephaly but with mild frontal bossing. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
2 |
A form of non-syndromic multisutural craniosynostosis characterised by premature fusion of the bicoronal and metopic sutures, resulting in brachycephaly and trigonocephaly. |
Finding site |
True |
Structure of frontal suture of skull |
Inferred relationship |
Some |
3 |