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73117003: Sphenoid bone structure (body structure)


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

Descriptions:

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
2754751000005112 Struktur af os sphenoidale da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


60 descendants. Search Descendants:

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 del af neurokraniet som helhed false Additional relationship Some
Sphenoid bone structure Is a struktur af neurokraniet 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 Is a False Sphenoid bone structure Inferred relationship Some
Osteomyelitis of sphenoid bone Finding site False Sphenoid bone structure Inferred relationship Some 1
Acute osteomyelitis 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
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 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
A rare genetic syndromic intellectual disability affecting males with characteristics of short stature, mild to moderate intellectual deficits, craniofacial dysmorphism (prominent broad 'square' forehead, hypertelorism, depressed nasal bridge, broad nasal tip and anteverted nares) and early hypotonia present only until the age of 2. There have been no further descriptions in the literature since the original article in 1991 and it has been suggested that this condition represents an example of FG syndrome. 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
A rare developmental defect during embryogenesis disorder with characteristics of 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, and increased density of upper eyelashes, anteverted nares, abnormal dentition and capillary haemangioma. Finding site False Sphenoid bone structure Inferred relationship Some 2
A rare developmental defect during embryogenesis syndrome with characteristics of 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
A rare developmental defect during embryogenesis disorder with characteristics of 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, and increased density of upper eyelashes, anteverted nares, abnormal dentition and capillary haemangioma. Finding site True Sphenoid bone structure Inferred relationship Some 1
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of 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 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)

US English

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