107656002: Congenital anomaly (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

172092016 Congenital anomaly en Synonym Active Entire term case insensitive SNOMED CT core module

593259012 Congenital anomaly (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital anomaly	Is a	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier
Congenital anomaly	Is a	Developmental anomaly	false	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital abnormal fusion of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Other fallopian tube and broad ligament anomalies	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Baller-Gerold syndrome	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Acrosyndactyly of thumb	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Brachycephaly	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Spina bifida aperta of thoracic spine	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital hypertrophy of sphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital spondylolisthesis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Spheno-fronto-parietal craniofaciosynostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital abnormal fusion of exoccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Embryonic cyst of fallopian tube or broad ligament NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital abnormal shape of alisphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital absence of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Acrocephalosyndactyly type V	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital abnormal fusion of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords at crest ventricular septum	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Congenital abnormal fusion of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital fenestration of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of parietal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal shape of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Incomplete ossification of alisphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital absence of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital hypoplasia of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Other fallopian tube or broad ligament anomalies NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords to papillary muscle on right ventricular side septum	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Atrioventricular septal defect with ventricular component under free floating superior bridging leaflet and chords to papillary muscle at right ventricular free wall	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Fallopian tube or broad ligament anomalies NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Cerebrovascular system anomaly NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Amyoplasia congenita disruptive sequence	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Fallopian tube and broad ligament anomalies, unspecified	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital anomaly of parietal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Prepapillary vascular loop	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Cerebrovascular system anomalies	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Incomplete ossification of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Fronto-parietal craniofaciosynostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Imperfect fusion of skull	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Ullrich-Feichtiger syndrome, chimera	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Apert's syndrome	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	4
Congenital hypoplasia of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal fusion of parietal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital arteriovenous malformation of gastrointestinal tract	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal shape of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Incomplete ossification of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Cloverleaf skull syndrome	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Congenital spondylolisthesis of cervical vertebra	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Incomplete ossification of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Atrioventricular septal defect - ventricular component under superior bridging leaflet	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Congenital hypoplasia of exoccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital hypoplasia of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Vomero-premaxillary faciosynostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital generalized flexion contractures of lower limb joints	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Fronto-frontal dysostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Spheno-frontal dysostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Parieto-occipital craniosynostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of cerebral vessel, unspecified	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Other specified cerebrovascular anomaly	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
[X]Other congenital malformations of fallopian tube and broad ligament	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
[X]Other congenital malformations of fallopian tube and broad ligament	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Fallopian tube and broad ligament anomalies	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Fallopian tube and broad ligament anomalies, unspecified	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Embryonic cyst of fallopian tube or broad ligament NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Other fallopian tube and broad ligament anomalies	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Other fallopian tube or broad ligament anomalies NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Fallopian tube or broad ligament anomalies NOS	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormality of atrioventricular valves in atrioventricular septal defect	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Atrioventricular septal defect - isolated ventricular component	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Atrioventricular septal defect: atrial and ventricular components	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Atrioventricular septal defect - ventricular component under inferior bridging leaflet	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Reconstruction of radial club hand	Direct morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Mittendorf's dot	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital vascular anomaly of eye	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Schprintzen	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Trigonocephaly	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Crouzon syndrome	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Unicoronal craniosynostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Bicoronal craniosynostosis	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Acrosyndactyly of thumb	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Repair of interrupted aortic arch	Direct morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	1
Persistent hyaloid artery	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Spina bifida aperta of cervical spine	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal shape of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital abnormal shape of squamosal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal shape of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital fenestration of alisphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of alisphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of basioccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of exoccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of frontal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital hypoplasia of alisphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital hypoplasia of frontal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal fusion of alisphenoid bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal fusion of frontal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormal fusion of lacrimal bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital abnormal fusion of vomer	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	3
Congenital abnormal shape of exoccipital bone	Associated morphology	False	Congenital anomaly	Inferred relationship	Existential restriction modifier	2

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Id	Description	Lang	Type	Status	Case?	Module
172092016	Congenital anomaly	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
593259012	Congenital anomaly (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module