21390004: Developmental anomaly (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
dysgenese	Is a	kongenit anomali	false	Inferred relationship	Some
dysgenese	Is a	Morphologically abnormal structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital enlarged kidney	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Partial agenesis of pericardium (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Class III buccal segment relationship - half unit	Associated morphology	False	dysgenese	Inferred relationship	Some	4
Buccal maxillary posterior crossbite (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	1
Single ventricular outlet above right ventricle (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Duplex kidney with reflux in one ureter (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
uterus bicornis, barn født	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Cleft lip sequence	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Congenital malformation of salivary glands and ducts	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Multiple intracardiac shunts	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Dental midlines coincident and incorrect	Associated morphology	False	dysgenese	Inferred relationship	Some	4
Tetralogy of Fallot	Associated morphology	False	dysgenese	Inferred relationship	Some	7
True generalized microdontia	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Double outlet right ventricle with subaortic ventricular septal defect	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Arterial anomaly of umbilical cord	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Amelogenesis imperfecta	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Accessory tissue on tricuspid leaflet	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Acephalostomia	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital abnormality of uterus in pregnancy, childbirth and the puerperium	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Midline deviation of dental arch	Associated morphology	False	dysgenese	Inferred relationship	Some	4
Right ventricular outflow tract obstruction due to septal hypertrophy (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Aortic orifice anterior left with respect to pulmonary orifice (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Double outlet right ventricle with noncommitted ventricular septal defect (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Left ventricular outflow tract obstruction due to diaphragm (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Diskoid nyre	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Incomplete bilateral cleft palate	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Abnormal atrioventricular connection	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Double urinary meatus (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital short urethra	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Left ventricular outflow tract obstruction due to aneurysm of membranous septum (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Precocious exfoliation due to ectopic eruption of proximate tooth (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Peg-shaped teeth	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Hypoplasia of right ventricular outflow tract and trabecular area	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Commissural fusion of aortic valve	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital anterior urethral valve	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Eisenmengers syndrom	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Overriding tricuspid valve (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Odontogenesis imperfecta	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Isomerism of left atrial appendage (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Bilateral isomeric atria (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Amelogenesis imperfecta - recessive - rough (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Congenital anomaly of the urinary tract proper (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Absent right sided atrioventricular connection	Associated morphology	False	dysgenese	Inferred relationship	Some	2
A rare heterotaxia characterised by complex congenital heart malformations and abnormal lateralisation of other thoracic and abdominal organs due to embryonic disruption of the left-right axis development. Cardiac defects include dextrocardia or mesocardia, common atrioventricular valve associated with complete atrioventricular septal defect or common atrium, transposition or malposition of the great arteries, and total anomalous pulmonary venous drainage, among others. Cardiac arrhythmias are frequently observed. Typical abnormalities of other organs are bilateral trilobed lungs, midline liver, and asplenia. Patients present in the newborn period with severe cardiac failure and cyanosis. Prognosis is poor.	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital anomaly of pericardium	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Stenosis of systemic to pulmonary artery collateral artery (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	4
Right ventricular outflow tract obstruction due to abnormal cardiac muscle bands (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Kohlschutter's syndrome	Associated morphology	False	dysgenese	Inferred relationship	Some	4
Complete bilateral cleft palate	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Double outlet right ventricle with subpulmonary ventricular septal defect (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Commissural fusion of pulmonary valve	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital abnormality of oral cavity	Associated morphology	False	dysgenese	Inferred relationship	Some	1
Solitary pulmonary trunk with aortic atresia	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Congenital lobulation of kidney	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Bilateral cleft lip	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Premature restriction of foramen ovale (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Posterior buccal occlusion of mandibular teeth	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Cleft palate	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital fusion of pulmonary valve segment	Associated morphology	False	dysgenese	Inferred relationship	Some	2
X-linked periventricular heterotopia (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Embryonic cyst of broad ligament	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital abnormality of relationship of cardiac component	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital abnormality of uterus, affecting pregnancy	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Ectopic gastric mucosa - multiple sites (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Amelogenesis imperfecta - hypomaturation - recessive pigmented	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Sekundært tab af tandbuelængde	Associated morphology	False	dysgenese	Inferred relationship	Some	1
Allantoic cyst	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Incomplete cleft hard and soft palate	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Obstruktion af højre ventrikels udløbsdel – tubulær	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Left sided atrium connecting to left ventricle (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Supernumerary pulmonary valve cusps	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Supernumerary deciduous maxillary tooth	Associated morphology	False	dysgenese	Inferred relationship	Some	1
Pulmonary valve dysplasia	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital anomaly of renal pelvis	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Criss-cross heart with rightward rotation (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Right ventricular outflow tract obstruction due to common atrioventricular valve (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Paroophoron	Associated morphology	False	dysgenese	Inferred relationship	Some	1
Byzanthine arch palate	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Myocardial bridge of coronary artery (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Brunner's gland adenoma	Associated morphology	False	dysgenese	Inferred relationship	Some	4
Congenital renal failure	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Quadricuspid cardiac valve	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Two chambered right ventricle (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Transient tricuspid regurgitation of newborn	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Double orifice of tricuspid valve	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital downward displacement of stomach	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Congenital abnormality of salivary duct (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Embedded tooth	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Right ventricular outflow tract absent (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Venous anomaly of umbilical cord	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Congenital cystic kidney disease	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Dentinogenesis imperfecta - Shield's type III	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Female epispadias (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Right ventricle to left of left ventricle (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Female infertility due to structural congenital anomaly of vagina	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Female infertility due to structural congenital anomaly of cervix (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Uterus unicornis	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Female hypospadias (disorder)	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Primary vesicoureteric reflux	Associated morphology	False	dysgenese	Inferred relationship	Some	2
Simple ureterocele	Associated morphology	False	dysgenese	Inferred relationship	Some	3
Anomalous cardiac muscle bands	Associated morphology	False	dysgenese	Inferred relationship	Some	2

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Id	Description	Lang	Type	Status	Case?	Module
183282017	Developmental anomaly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
190336012	Developmental malformation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
190337015	Developmental defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
190338013	Dysgenesis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
190339017	Anomalous formation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
190340015	Abnormal development	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
190341016	Malformation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
750678013	Developmental anomaly (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1208681014	Developmental abnormality	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2614401000005117	dysgenese	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)