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74872008: Frontal bone structure (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Structure of bone organ\Bone structure\...

\Structure of type of bone (body structure)\Structure of flat bone\Frontal bone structure

\Regional bone structure\Bone structure of head and/or neck (body structure)\Bone structure of head\Bone structure of cranium\Bone structure of neurocranium\Frontal bone structure

\Body system structure\Structure of musculoskeletal system (body structure)\...

\Skeletal system structure\Structure of bony skeleton\Bony skeleton subdivision\Bone structure\Structure of type of bone (body structure)\Structure of flat bone\Frontal bone structure
\Skeletal system structure\Structure of bony skeleton\Bony skeleton subdivision\Bone structure\Regional bone structure\Bone structure of head and/or neck (body structure)\Bone structure of head\Bone structure of cranium\Bone structure of neurocranium\Frontal bone structure
\Skeletal system structure\Bone and/or joint structure (body structure)\Bone structure\Structure of type of bone (body structure)\Structure of flat bone\Frontal bone structure
\Skeletal system structure\Bone and/or joint structure (body structure)\Bone structure\Regional bone structure\Bone structure of head and/or neck (body structure)\Bone structure of head\Bone structure of cranium\Bone structure of neurocranium\Frontal bone structure
\Skeletal system structure\Axial skeleton structure\Bone structure of head\Bone structure of cranium\Bone structure of neurocranium\Frontal bone structure

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Frontal bone structure	Is a	Neurocranium structure	false	Inferred relationship	Some
Frontal bone structure	partie de	Entire neurocranium	false	Additional relationship	Some
Frontal bone structure	Is a	Neurocranium structure	false	Inferred relationship	Some
Frontal bone structure	Is a	Structure of flat bone	true	Inferred relationship	Some
Frontal bone structure	Is a	Frontal region structure	true	Inferred relationship	Some
Frontal bone structure	Is a	Bone structure of neurocranium	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Structure of bone marrow of frontal bone	Is a	False	Frontal bone structure	Inferred relationship	Some
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	Frontal bone structure	Inferred relationship	Some	3
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	Frontal bone structure	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	Frontal bone structure	Inferred relationship	Some	6
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	Frontal bone structure	Inferred relationship	Some	4
Fracture of squama of frontal bone of skull (disorder)	Finding site	True	Frontal bone structure	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	Frontal bone structure	Inferred relationship	Some	2
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	Frontal bone structure	Inferred relationship	Some	3
Trigonocephaly	Finding site	True	Frontal bone structure	Inferred relationship	Some	1
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	Frontal bone structure	Inferred relationship	Some	4
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	Frontal bone structure	Inferred relationship	Some	1
Stewart-Morel-Morgagni syndrome (disorder)	Finding site	True	Frontal bone structure	Inferred relationship	Some	1
Spheno-frontal dysostosis	Finding site	True	Frontal bone structure	Inferred relationship	Some	2
Osteomyelitis of frontal bone	Finding site	True	Frontal bone structure	Inferred relationship	Some	2
Frontal encephalocele	Finding site	True	Frontal bone structure	Inferred relationship	Some	1
Isolated trigonocephaly is a nonsyndromic form of craniosynostosis characterised by the premature fusion of the metopic suture.	Finding site	True	Frontal bone structure	Inferred relationship	Some	1
Chronic osteomyelitis of frontal bone	Finding site	True	Frontal bone structure	Inferred relationship	Some	3
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	Frontal bone structure	Inferred relationship	Some	3
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	Frontal bone structure	Inferred relationship	Some	4

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

Description inactivation indicator reference set

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Id	Description	Lang	Type	Status	Case?	Module
124348014	Frontal bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
502839013	Frontal bone structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
815419016	Frontal bone structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
910801000172111	structure de l'os frontal	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
930311000172110	os frontal	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
985011000172112	os frontale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module