23416004: Bone structure of ulna (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 long bone\Structure of long bone of upper limb (body structure)\Structure of bone of forearm (body structure)\Bone structure of ulna

\Regional bone structure\Bone structure of limb\Bone structure of upper limb (body structure)\...

\Bone structure of free upper limb\Structure of bone of forearm (body structure)\Bone structure of ulna

\Structure of long bone of upper limb (body structure)\Structure of bone of forearm (body structure)\Bone structure of ulna

\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
Bone structure of ulna	Is a	Structure of long bone	false	Inferred relationship	Some
Bone structure of ulna	Is a	Structure of bone of forearm (body structure)	false	Inferred relationship	Some
Bone structure of ulna	partie de	Entire forearm	false	Additional relationship	Some
Bone structure of ulna	partie de	Entire bony skeleton	false	Additional relationship	Some
Bone structure of ulna	Is a	Radius and ulna (combined site) (body structure)	false	Inferred relationship	Some
Bone structure of ulna	Is a	Bone structure of forearm	false	Inferred relationship	Some
Bone structure of ulna	Is a	Structure of long bone of upper limb (body structure)	false	Inferred relationship	Some
Bone structure of ulna	Is a	Structure of bone of forearm (body structure)	true	Inferred relationship	Some
Bone structure of ulna	Laterality	Side (qualifier value)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Humeroulnar synostosis (disorder)	Finding site	False	Bone structure of ulna	Inferred relationship	Some	2
Infection of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	3
Plain X-ray of ulna (procedure)	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	2
Structure of bone marrow of ulna (body structure)	Is a	False	Bone structure of ulna	Inferred relationship	Some
Ulna metaphyseal dysplasia syndrome (disorder)	Finding site	False	Bone structure of ulna	Inferred relationship	Some	2
Fibulo-ulnar hypoplasia-renal anomalies syndrome is characterized by fibulo-ulnar dysostosis with renal anomalies. It has been described in two siblings born to non-consanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial anomalies (including micrognathia), symmetrical shortness of long bones, fibular agenesis and hypoplastic ulna, oligosyndactyly, congenital heart defects, and cystic or hypoplastic kidney. It is transmitted as an autosomal recessive trait.	Finding site	False	Bone structure of ulna	Inferred relationship	Some	5
Bone structure of left ulna (body structure)	Is a	True	Bone structure of ulna	Inferred relationship	Some
Bone structure of right ulna (body structure)	Is a	True	Bone structure of ulna	Inferred relationship	Some
Ulna hypoplasia - intellectual deficit is a very rare syndrome characterized by mesomelic shortness of the forearms, bilateral clubfeet, aplasia or hypoplasia of all nails and severe psychomotor retardation.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
A rare congenital malformation syndrome characterized by ulnar hypoplasia associated with hypoplastic to absent fourth and/or fifth digits, fibular hypoplasia, short stature and facial dysmorphism.	Finding site	False	Bone structure of ulna	Inferred relationship	Some	7
A rare congenital malformation syndrome characterized by ulnar hypoplasia associated with hypoplastic to absent fourth and/or fifth digits, fibular hypoplasia, short stature and facial dysmorphism.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	4
Ulnar hypoplasia-split foot syndrome is characterized by the association of severe ulnar hypoplasia, absence of fingers two to five, and split-foot. It has been described in four males belonging to two generations of the same family. X-linked recessive inheritance is suggested, but autosomal dominant transmission cannot be excluded.	Finding site	False	Bone structure of ulna	Inferred relationship	Some	5
Congenital absence of forearm and hand	Finding site	False	Bone structure of ulna	Inferred relationship	Some	5
Spondyloperipheral dysplasia-short ulna syndrome is a rare, genetic, primary bone dysplasia, with highly variable phenotype, typically characterized by platyspondyly, brachydactyly type E changes (short metacarpals and metatarsals, short distal phalanges in hands and feet), bilateral short ulnae and mild short stature. Other reported features include additional skeletal findings (e.g. midface hypoplasia, degenerative changes in proximal femora, limited elbow extension, bilateral sacralization of L5, clubfeet), as well as myopia, hearing loss, and intellectual disability.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Pathologic fracture of ulna at site of neoplasm	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Ulna metaphyseal dysplasia syndrome (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Fibulo-ulnar hypoplasia-renal anomalies syndrome is characterized by fibulo-ulnar dysostosis with renal anomalies. It has been described in two siblings born to non-consanguinous parents. The syndrome is lethal at birth (respiratory failure). Clinical manifestations include ear and facial anomalies (including micrognathia), symmetrical shortness of long bones, fibular agenesis and hypoplastic ulna, oligosyndactyly, congenital heart defects, and cystic or hypoplastic kidney. It is transmitted as an autosomal recessive trait.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Ulnar hypoplasia-split foot syndrome is characterized by the association of severe ulnar hypoplasia, absence of fingers two to five, and split-foot. It has been described in four males belonging to two generations of the same family. X-linked recessive inheritance is suggested, but autosomal dominant transmission cannot be excluded.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
Congenital absence of forearm and hand	Finding site	False	Bone structure of ulna	Inferred relationship	Some	3
A rare congenital malformation syndrome characterized by ulnar hypoplasia associated with hypoplastic to absent fourth and/or fifth digits, fibular hypoplasia, short stature and facial dysmorphism.	Finding site	False	Bone structure of ulna	Inferred relationship	Some	3
Plain X-ray for ulnar variance view (procedure)	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Short ulna-dysmorphism-hypotonia-intellectual disability syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by mild to severe global development delay, severe intellectual disability, mild hypotonia, a short ulna, hirsutism of the face and extremities, minimal scoliosis, and facial dysmorphism, notably a tall broad forehead, synophrys, hypertelorism, malar hypoplasia, broad nose with thick alae nasi, low-set, small ears, long philtrum, thin upper lip and everted lower lip vermilion.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Humero-radio-ulnar synostosis is an extremely rare, genetic, congenital joint formation defect disorder characterized by uni- or bilateral fusion of the humerus, radius and ulnar bones, leading to loss of elbow motion and, in most, functional arm incapacity. It may appear as distal humeral bifurcation with absent elbow joint and shortened arm length on imaging. Hand abnormalities, namely oligoectrosyndactyly, may be associated.	Finding site	False	Bone structure of ulna	Inferred relationship	Some	3
Congenital absence of left forearm and hand (disorder)	Finding site	False	Bone structure of ulna	Inferred relationship	Some	4
Congenital absence of right forearm and hand	Finding site	False	Bone structure of ulna	Inferred relationship	Some	4
Congenital bowing of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Radioulnar synostosis-microcephaly-scoliosis syndrome, also known as Guiffré-Tsukahara syndrome, is an extremely rare syndrome characterized by the association of radioulnar synostosis with microcephaly, scoliosis, short stature and intellectual deficit.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	3
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	Bone structure of ulna	Inferred relationship	Some	1
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome is characterized by the association of proximal fusion of the radius and ulna with congenital amegakaryocytic thrombocytopenia. Less than 10 cases have been reported in the literature so far. The syndrome is transmitted as an autosomal dominant trait and is caused by mutations in the HOXA11 gene (7p15).	Finding site	False	Bone structure of ulna	Inferred relationship	Some	3
Radioulnar synostosis-developmental delay-hypotonia syndrome, also known as Der Kaloustian-McIntosh-Silver syndrome, is an extremely rare syndrome with synostosis described in about 4 patients to date with clinical manifestations including congenital unilateral radioulnar synostosis, generalized hypotonia, developmental delay, and dysmorphic facial features (long face, prominent nose and ears).	Finding site	False	Bone structure of ulna	Inferred relationship	Some	3
Operation for injury of radius AND ulna	Procedure site	True	Bone structure of ulna	Inferred relationship	Some	1
Secondary osteoporotic fracture of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Osteoporotic fracture of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Osteotomy of radius and ulna	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Arthrodesis of distal radioulnar joint and segmental resection of ulna with bone graft (procedure)	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	3
Grafting of bone of ulna	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Grafting of bone of ulna	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	2
Excision of radius AND ulna for graft	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	3
Arthrodesis of distal radioulnar joint and segmental resection of ulna with bone graft (procedure)	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	4
Bone graft of radius and ulna	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	3
Bone graft of radius and ulna	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Periosteal suture of ulna	Procedure site - Indirect (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Mesomelic dysplasia of upper limb (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Brachydactyly-mesomelia-intellectual disability-heart defects syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, thin habitus with narrow shoulders, mesomelic shortness of the arms, craniofacial dysmorphism (e.g. long lower face, maxillary hypoplasia, beak nose, short columella, prognathia, high arched palate, obtuse mandibular angle), brachydactyly (mostly involving middle phalanges) and cardiovascular anomalies (i.e. aortic root dilatation, mitral valve prolapse).	Finding site	True	Bone structure of ulna	Inferred relationship	Some	5
Mesomelic dysplasia, Savarirayan type is characterized by severely hypoplastic and triangular-shaped tibiae, and absence of the fibulae. So far, two sporadic cases have been described. Moderate mesomelia of the upper limbs, proximal widening of the ulnas, pelvic anomalies and marked bilateral glenoid hypoplasia were also reported.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
A rare disorder characterized by disproportionate short stature from birth with dysplasia of the ulna and fibula.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	5
Congenital radioulnar synostosis	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Radioulnar synostosis following traumatic injury (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Surgical lengthening of radius and ulna with autografts (procedure)	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	2
Osteitis deformans of radius and ulna (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Osteomyelitis of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Plain X-ray of radius and ulna (procedure)	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Plain X-ray of radius and ulna normal	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
Plain X-ray of ulna normal	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
Plain X-ray of radius and ulna abnormal	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
Plain X-ray of ulna abnormal	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
Exostosis of ulna (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome is characterized by the association of proximal fusion of the radius and ulna with congenital amegakaryocytic thrombocytopenia. Less than 10 cases have been reported in the literature so far. The syndrome is transmitted as an autosomal dominant trait and is caused by mutations in the HOXA11 gene (7p15).	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Radioulnar synostosis-developmental delay-hypotonia syndrome, also known as Der Kaloustian-McIntosh-Silver syndrome, is an extremely rare syndrome with synostosis described in about 4 patients to date with clinical manifestations including congenital unilateral radioulnar synostosis, generalized hypotonia, developmental delay, and dysmorphic facial features (long face, prominent nose and ears).	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Humero-radio-ulnar synostosis is an extremely rare, genetic, congenital joint formation defect disorder characterized by uni- or bilateral fusion of the humerus, radius and ulnar bones, leading to loss of elbow motion and, in most, functional arm incapacity. It may appear as distal humeral bifurcation with absent elbow joint and shortened arm length on imaging. Hand abnormalities, namely oligoectrosyndactyly, may be associated.	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Hypertrophy of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Solitary bone cyst of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Avascular necrosis of ulna (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Enostosis of ulna (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Prophylactic treatment of radius and ulna with methyl methacrylate	Procedure site - Direct (attribute)	True	Bone structure of ulna	Inferred relationship	Some	1
Disorder of bone and cartilage of ulna (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	2
Aplasia of ulna	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1
Congenital abnormal slender shape of ulna (disorder)	Finding site	True	Bone structure of ulna	Inferred relationship	Some	1

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

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

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

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Id	Description	Lang	Type	Status	Case?	Module
39313010	Ulna	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
481615013	Bone structure of ulna	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
752934010	Bone structure of ulna (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
909361000172114	structure osseuse de l'ulna	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
911251000172118	os ulnaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
913881000172111	os cubital	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
931671000172116	cubitus	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1014421000172115	ulna	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module