107656002: Congenital anomaly (morphologic abnormality)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
anomalie congénitale	Is a	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
anomalie congénitale	Is a	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Right ventricle outflow chamber	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Intra-articular soft tissue procedure for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Extra-articular soft tissue procedure for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Osteotomy of ilium for correction of congenital deformity of hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Salter osteotomy for congenital deformity of hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Chiari osteotomy for congenital deformity of hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Colonna osteotomy for congenital deformity of hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Other specified correction of congenital deformity of hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Excision of anlage of fibula	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Centralisation tarsus correction	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
ostéoplastie de retournement de la cheville	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Gruca tibial bifurcation procedure (procedure)	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Creation of tibiofibular synostosis	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Other specified correction of congenital deformity of leg	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Correction of congenital deformity of leg NOS	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Soft tissue procedure for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Triple pelvic osteotomy for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Correction of tibial pseudoarthrosis by DCIA (deep circumflex iliac artery) bone flap	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Correction of tibial pseudoarthrosis by excision and bone lengthening (procedure)	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Persistence of primitive artery (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Persistent cerebral embryonic artery	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Cystic fibrosis of pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amelogenesis imperfecta - recessive - rough	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amelogenesis imperfecta - hypomaturation - recessive pigmented	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amelogenesis imperfecta - hypomaturation - snow capped teeth	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Unspecified anomaly of heart valve	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other specified anomaly of pulmonary artery	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other anomaly of trachea	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other anomaly of bronchus	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other pharynx anomalies	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other pharynx anomalies NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other specified upper alimentary tract anomaly	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Upper alimentary tract anomalies NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomalies of pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Other specified anomalies of pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Obstructive defect of renal pelvis or ureter NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital sacrococcygeal anomalies NEC	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital sacrococcygeal anomaly NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital malformation syndromes with other skeletal changes	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
[X]Other congenital malformations of pancreas and pancreatic duct	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Septal defect NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary osteotomy of pelvis for correction of congenital deformity of hip (procedure)	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pelvic osteotomy for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomalies of upper alimentary tract NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fusion of tricuspid valve cusps NEC	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreas divisum - complete (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of peripheral blood vessel	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of blood vessel of upper limb (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Islet cell hyperplasia	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital anomaly of renal blood vessel (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amelogenesis imperfecta (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Karyotype 46, X iso (Xq)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Correction of tibial pseudoarthrosis by DCIA (deep circumflex iliac artery) bone flap	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Turner's phenotype, partial X deletion karyotype (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Right sided atrium connecting to ventricle of indeterminate morphology	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital absence of pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Correction of tibial pseudoarthrosis by excision and bone lengthening (procedure)	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mosaicism 45, X / other cell line with abnormal sex chromosome	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Other specified correction of congenital deformity of leg	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of peripheral blood vessel	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Correction of congenital deformity of foot	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Correction of congenital deformity of leg NOS	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Atresia of heart valve NEC	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Annular pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Persistence of primitive artery (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Karyotype 46, X with abnormal sex chromosome except iso (Xq)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Septal defect NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
arthroplastie secondaire de la hanche pour correction d'une malformation congénitale	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital abnormalities of thoracic aortic branches	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Gynandromorphism syndrome	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Cutis marmorata	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pulmonary artery anomaly NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fusion of tricuspid valve cusps NEC	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital malformation syndrome with other skeletal changes NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other specified anomaly of pulmonary artery	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Four X syndrome	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Rud's syndrome	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital malformation syndromes with other skeletal changes	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other specified obstructive defect of renal pelvis or ureter	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Upper alimentary tract anomalies NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital anomaly of renal blood vessel (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
dystrophie endothéliale congénitale héréditaire type I	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital insufficiency of heart valve NEC	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Complete trisomy 13 syndrome (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomalies of pancreas	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Diaphragm anomalies NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sturge-Weber syndrome (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Other pharynx anomalies NOS	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fusion of heart valve cusps NEC	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hereditary endothelial dystrophy type 2 (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)
Pelvic osteotomy for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Extra-articular soft tissue procedure for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Soft tissue procedure for congenital dislocation of the hip	Direct morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital anomaly of the urinary tract	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Accessory pancreas (disorder)	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)	2
13q partial monosomy syndrome	Associated morphology	False	anomalie congénitale	Inferred relationship	Existential restriction modifier (core metadata concept)

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Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set

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Id	Description	Lang	Type	Status	Case?	Module
172092016	Congenital anomaly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
593259012	Congenital anomaly (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
172092016	Congenital anomaly	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
172092016	Congenital anomaly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
593259012	Congenital anomaly (morphologic abnormality)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
593259012	Congenital anomaly (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
280471000077112	anomalie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
280471000077112	anomalie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module