37764001: Congenital abnormal fusion (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
kongenit abnorm sammenvoksning	Is a	kongenit anomali	false	Inferred relationship	Some
kongenit abnorm sammenvoksning	Is a	Fusion	false	Inferred relationship	Some
kongenit abnorm sammenvoksning	Is a	Kongenit malformation	false	Inferred relationship	Some
kongenit abnorm sammenvoksning	Is a	dysgenese	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cloverleaf skull syndrome (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Cleft hand with syndactyly	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Acrocephalopolysyndactyly	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Fusion of mandibular incisor teeth (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Antley-Bixler syndrome	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Antley-Bixler syndrome	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Antley-Bixler syndrome	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	7
Antley-Bixler syndrome	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	8
Humeroradial synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Humeroradial synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Anadidymus	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Distal radioulnar synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Ulnar og humeroulnar synostose	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Ulnar og humeroulnar synostose	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Proximal radioulnar synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Humeroulnar synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Humeroulnar synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Imperfect fusion of skull	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Congenital fusion of labia	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Commissural fusion of aortic valve	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Commissural fusion of pulmonary valve	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Congenital fusion of pulmonary valve segment	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Congenital fusion of spine	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital lumbosacral fusion	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital partial fusion of spine with hemivertebra - unbalanced	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Constriction ring of upper limb with acrosyndactyly and amputation	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital synostosis of lower limb bones	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Congenital fusion of pulmonic cusps	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Congenital partial fusion of spine - unbalanced	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital fusion of ossicles of ear	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Congenital complete fusion of spine	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital complete fusion of spine	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Supernumerary fused sternebra	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Acrosyndactyly of thumb (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Naviculocuneiform bar	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Radioulnar synostosis and dislocation of radial head	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	6
Congenital fusion of sacroiliac joint (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Congenital fusion of sacroiliac joint (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	6
Congenital partial fusion of spine	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Talocalcaneal coalition	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital fusion of testis (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Astragaloscaphoid synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Calcaneonavicular bar	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital partial fusion of spine - balanced	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
A congenital differentiation of the fifth lumbar vertebra (L5) such that it takes on characteristics of a sacral vertebra. Though the sacralization is usually incomplete and limited to one side, it can be partial or complete on one or both sides of the sacrum	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Lumbarized first sacral vertebra	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital partial fusion of spine with hemivertebra - balanced	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Complex tarsal coalition	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Congenital fusion of ribs	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
A congenital differentiation of the fifth lumbar vertebra (L5) such that it takes on characteristics of a sacral vertebra. Though the sacralization is usually incomplete and limited to one side, it can be partial or complete on one or both sides of the sacrum	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	6
Imperfect fusion of skull	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Horseshoe kidney	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Assimilation pelvis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Splenogonadal fusion	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Pygopagus	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Omphalopagus	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Congenital fusion of pulmonary valve segment	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Simple syndactyly of toes	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Osseous syndactyly lesser toes	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Lunate-triquetrum synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Capitate-hamate synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Scaphoid-lunate synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Humeroulnar synostosis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Congenital synostosis of lower limb bones	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Congenital complete fusion of spine	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Commissural fusion of pulmonary valve	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Commissural fusion of aortic valve	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Acrosyndactyly of the fingers	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Karpalsynostose	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Brachysyndactyly of thumb	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Ossøs syndaktyli i tæer, 2. til 4. tåmellemrum	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Syndactyly of thumb (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Congenital fusion of labia	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Supernumerary fused sternebra	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Coloboma of choroid	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	7
Cake kidney	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Craniopagus parietalis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Craniopagus	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Craniopagus occipitalis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Craniopagus frontalis	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Craniopagus parasiticus	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Splenogonadal fusion	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Fundus coloboma	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Syndactyly of fingers type 8 (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
Laurin-Sandrow syndrome (LSS) is characterized by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
A rare non-syndromic syndactyly characterized by complete or partial webbing between the 3rd and 4th fingers and/or the 2nd and 3rd toes. Other digits may be involved occasionally. The phenotype varies widely within and between families, sometimes only the hands are affected and sometimes only the feet. Webbing between fingers may be associated with bony fusion of the distal phalanges.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
A rare non-syndromic syndactyly characterized by complete and bilateral syndactyly between the 4th and 5th fingers. In most cases, it is a soft tissue syndactyly, but occasionally the distal phalanges may be fused. The middle phalanx of the fifth finger is usually hypoplastic, and the feet are not affected.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
A rare non-syndromic syndactyly characterized by a distinctive combination of syndactyly and polydactyly, generally affecting the 3rd and 4th fingers and the 4th and 5th toes, bilaterally, with partial or complete reduplication of a digital ray within the syndactylous web. Additional features include 5th finger clinodactyly, camptodactyly and/or brachydactyly.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Microcephaly-cervical spine fusion anomalies syndrome is characterized by microcephaly, facial dysmorphism (beaked nose, low-set ears, downslanting palpebral fissures, micrognathia), mild intellectual deficit, short stature, and cervical spine fusion anomalies producing spinal cord compression. It has been described in two brothers born to consanguineous parents. Transmission is likely to be autosomal recessive.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
A rare non-syndromic syndactyly characterized by complete bilateral cutaneous fusion of all fingers, frequently associated with polydactyly (usually involving six digits and six metacarpals). Phalanges may fuse as a conglomerate mass of bones. Feet are occasionally affected.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
A rare non-syndromic syndactyly characterized by soft tissue syndactyly of the 3rd and 4th fingers and the 2nd and 3rd toes associated with metacarpal and metatarsal fusion of the 4th and 5th digits. Shortening of fused metacarpals, ulnar deviation of fingers, interdigital cleft, camptodactyly, short distal phalanges, and absent distal interphalangeal creases have also been reported.	Associated morphology	False	kongenit abnorm sammenvoksning	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.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	5
Progressive non-infectious anterior vertebral fusion (PAVF) is an early childhood spinal disorder characterized by the gradual onset of thoracic and/or lumbar spine ankylosis often in conjunction with kyphosis with distinctive radiological features.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
A rare congenital malformation syndrome characterized by cleft soft palate, severe oligodontia of the deciduous teeth, absence of the permanent dentition, bilateral conductive deafness due to fixation of the footplate of the stapes, short halluces with a wide space between the first and second toes, and fusion of carpal and tarsal bones. There have been no further descriptions in the literature since 1971.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Triphalangeal thumb and polysyndactyly syndrome (disorder)	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
A rare syndrome characterized by a combination of distal limb abnormalities (syndactyly of all fingers and toes, preaxial polydactyly in the feet and/or hands) and upper sternum malformations.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Brachydactyly-syndactyly, Zhao type is a recently described syndrome associating a brachydactyly type A4 (short middle phalanges of the 2nd and 5th fingers and absence of middle phalanges of the 2nd to 5th toes) and a syndactyly of the 2nd and 3rd toes. Metacarpals and metatarsals anomalies are common.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	3
Cenani-Lenz syndrome (CLS) is a congenital malformation syndrome that associates a complex syndactyly of the hands with malformations of the forearm bones and similar manifestations in the lower limbs.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	1
An extremely rare malformation syndrome characterized by the association of partial distal aphalangia with syndactyly, duplication of metatarsal IV, microcephaly, and mild intellectual disability.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4
Brachydactyly-syndactyly, Zhao type is a recently described syndrome associating a brachydactyly type A4 (short middle phalanges of the 2nd and 5th fingers and absence of middle phalanges of the 2nd to 5th toes) and a syndactyly of the 2nd and 3rd toes. Metacarpals and metatarsals anomalies are common.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	2
Craniosynostosis, Philadelphia type is a form of syndromic craniosynostosis, characterized by sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. Craniosynostosis, Philadelphia type has been suggested to share the same etiology as syndactyly type 1A.	Associated morphology	False	kongenit abnorm sammenvoksning	Inferred relationship	Some	4

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Id	Description	Lang	Type	Status	Case?	Module
62997012	Congenital abnormal fusion	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
63002015	Congenitally fused structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
63003013	Congenital failure of segmentation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
63004019	Congenital failure of cleavage	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
769668015	Congenital abnormal fusion (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2676631000005113	kongenit abnorm sammenvoksning	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)