73117003: Sphenoid 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 irregular bone (body structure)\Structure of pneumatic bone\Sphenoid 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\Sphenoid bone structure

\Body system structure\Structure of musculoskeletal system (body 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
Sphenoid bone structure	Is a	Neurocranium structure	false	Inferred relationship	Some
Sphenoid bone structure	partie de	Entire neurocranium	false	Additional relationship	Some
Sphenoid bone structure	Is a	Neurocranium structure	false	Inferred relationship	Some
Sphenoid bone structure	Is a	Structure of pneumatic bone	true	Inferred relationship	Some
Sphenoid bone structure	Is a	Bone structure of neurocranium	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Entire sphenoid bone	Is a	True	Sphenoid bone structure	Inferred relationship	Some
Sphenoid bone part	Is a	True	Sphenoid bone structure	Inferred relationship	Some
Structure of clinoid process of sphenoid bone	Is a	False	Sphenoid bone structure	Inferred relationship	Some
Structure of body of sphenoid bone (body structure)	Is a	False	Sphenoid bone structure	Inferred relationship	Some
Osteomyelitis of sphenoid bone (disorder)	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Acute osteomyelitis of sphenoid bone (disorder)	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Chronic osteomyelitis of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Chronic sclerosing nonsuppurative osteomyelitis of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Abscess of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Avascular necrosis of sphenoid bone caused by ionizing radiation (disorder)	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Sequestrum of the sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Sphenoidal dysostosis	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Spheno-frontal dysostosis	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Sphenoid sinus fracture	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Neoplasm of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Hypertelorism	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Congenital hypertrophy of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Fracture of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Benign neoplasm of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Primary malignant neoplasm of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Metastatic malignant neoplasm to sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Neoplasm of uncertain behavior of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Bone tissue of sphenoid bone	Is a	False	Sphenoid bone structure	Inferred relationship	Some
Abscess of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Neoplasm of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Acute osteomyelitis of sphenoid bone (disorder)	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Sequestrum of the sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Metastatic malignant neoplasm to sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Spheno-frontal dysostosis	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Fracture of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Hypertelorism	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Sphenoidal dysostosis	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Primary malignant neoplasm of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Neoplasm of uncertain behavior of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Avascular necrosis of sphenoid bone caused by ionizing radiation (disorder)	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Chronic sclerosing nonsuppurative osteomyelitis of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Benign neoplasm of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Congenital hypertrophy of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Chronic osteomyelitis of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	1
Congenital hypertrophy of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	2
Congenital hypertrophy of sphenoid bone	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	3
Hypertelorism	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	2
Congenital hypertrophy of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
Structure of bone marrow of sphenoid bone (body structure)	Is a	False	Sphenoid bone structure	Inferred relationship	Some
Hypertelorism-microtia-facial clefting syndrome, or HMC syndrome, is a very rare syndrome characterized by the combination of hypertelorism, cleft lip and palate and microtia.	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	5
Hypertelorism-microtia-facial clefting syndrome, or HMC syndrome, is a very rare syndrome characterized by the combination of hypertelorism, cleft lip and palate and microtia.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	4
A rare autosomal dominant malformation syndrome characterized by hypertelorism, omphalocoele, cleft lip, ear pits, uterine malformation (bicornuate uterus), and more variably by diaphragmatic hernia and congenital heart defects.	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	3
Hypospadias, hypertelorism, coloboma, deafness syndrome	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	7
Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia.	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	6
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the common manifestations found in oromandibular-limb hypogenesis syndromes (OLHS) group such as hypoplasia of the mandible, variable limb anomalies like syndactyly and ectrodactyly, small mouth, cleft palate and hypodontia, accompanied by other clinical signs such as facial paralysis, facial asymmetry, hypertelorism, hypoglossia/aglossia, absent or conically crowned incisors and, ectromelia. There have been no further descriptions in the literature since 1976.	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	4
Telecanthus-hypertelorism-strabismus-pes cavus syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and other variable anomalies. It has been described in a father and his son. The son also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of the fingers, and radiographic findings including flared metaphyses of the long bones and osteopenia.	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	5
Intellectual disability-short stature-hypertelorism syndrome is a rare genetic syndromic intellectual disability characterized by short stature, mild to moderate intellectual disability, craniofacial dysmorphism (prominent broad 'square' forehead, hypertelorism, depressed nasal bridge, broad nasal tip and anteverted nares) and early hypotonia, typically present until infancy. There have been no further descriptions in the literature since 1991.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	2
Hypospadias, hypertelorism, coloboma, deafness syndrome	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	2
Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	3
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the common manifestations found in oromandibular-limb hypogenesis syndromes (OLHS) group such as hypoplasia of the mandible, variable limb anomalies like syndactyly and ectrodactyly, small mouth, cleft palate and hypodontia, accompanied by other clinical signs such as facial paralysis, facial asymmetry, hypertelorism, hypoglossia/aglossia, absent or conically crowned incisors and, ectromelia. There have been no further descriptions in the literature since 1976.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	3
Telecanthus-hypertelorism-strabismus-pes cavus syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and other variable anomalies. It has been described in a father and his son. The son also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of the fingers, and radiographic findings including flared metaphyses of the long bones and osteopenia.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	2
A rare autosomal dominant malformation syndrome characterized by hypertelorism, omphalocoele, cleft lip, ear pits, uterine malformation (bicornuate uterus), and more variably by diaphragmatic hernia and congenital heart defects.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	2
Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome is a rare developmental defect during embryogenesis disorder characterized by macroblepharon, ectropion, and facial dysmorphism which includes severe hypertelorism, downslanting palpebral fissures, posteriorly rotated ears, broad nasal bridge, long and smooth philtrum, and macrostomia with thin upper lip vermilion border. Other features may include large fontanelles, prominent metopic ridge, thick eyebrows, mild synophrys, increased density of upper eyelashes, anteverted nares, abnormal dentition and capillary hemangioma.	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	2
A rare developmental defect during embryogenesis syndrome characterized by hypertelorism, bilateral preauricular sinus, bilateral punctal pits, lacrimal duct obstruction, hearing loss, abnormal palmar flexion creases and bilateral distal axial triradii. Shawl scrotum has also been reported.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	2
Spheno-frontal dysostosis	Finding site	False	Sphenoid bone structure	Inferred relationship	Some	2
Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome is a rare developmental defect during embryogenesis disorder characterized by macroblepharon, ectropion, and facial dysmorphism which includes severe hypertelorism, downslanting palpebral fissures, posteriorly rotated ears, broad nasal bridge, long and smooth philtrum, and macrostomia with thin upper lip vermilion border. Other features may include large fontanelles, prominent metopic ridge, thick eyebrows, mild synophrys, increased density of upper eyelashes, anteverted nares, abnormal dentition and capillary hemangioma.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	1
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by the triad: congenital, bilateral, symmetrical, subtotal, external auditory canal atresia, bilateral vertical talus and increased interocular distance.	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	2
Osteomyelitis of sphenoid bone (disorder)	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	2
Chronic osteomyelitis of sphenoid bone	Finding site	True	Sphenoid bone structure	Inferred relationship	Some	3

Reference Sets

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

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

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US English

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Id	Description	Lang	Type	Status	Case?	Module
121435010	Sphenoid bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
502359016	Sphenoid bone structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
813470011	Sphenoid bone structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
967021000172113	sphénoïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
972831000172111	os sphénoïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1000461000172117	structure de l'os sphénoïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1018181000172115	os sphenoidale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module