21390004: Developmental anomaly (morphologic abnormality)

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

Descriptions:

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cleft of alveolar ridge	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Angioma serpiginosum	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Congenital ringed hair	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital pulmonary artery conduit	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Isolation of branch of aortic arch	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Congenital anomaly of gastrointestinal tract	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Abnormal plantar creases	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormality of supraaortic branch of thoracic aorta	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Developmental immaturity	Is a	False	Developmental anomaly	Inferred relationship	Existential restriction modifier
Ash leaf spot, tuberous sclerosis	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Anonychia with bizarre flexural pigmentation	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Von Hippel-Lindau syndrome	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Imperforate esophagus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Bronchopulmonary collateral artery	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Autosomal dominant familial wooly hair	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital prognathism	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Coronary orifice asymmetrical	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Saddle nose	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Persistent aortic arch convolutions	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Meckel's diverticulum	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Temporal encephalocele	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Ichthyosis, cerebellar degeneration and hepatosplenomegaly	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Widely spaced right coronary artery and left coronary artery orifices within single aortic sinus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital endaural hernia	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Aortic tunnel	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of squamosal bone	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Anomalous pulmonary venous drainage to abdominal portion of inferior vena cava	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Congenital maxillary hyperplasia	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Microgenia	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Localized abdominal wall skin atrophy	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Incomplete ossification of palatine bone	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of alisphenoid bone	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Retroesophageal aortic arch	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Total anomalous pulmonary venous return	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital partial portal-systemic shunt	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Bilateral ductus arteriosus with closed left ductus arteriosus and patent right ductus arteriosus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Lack of ossification of zygomatic bone	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Abnormal dermatoglyphic pattern	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital abnormalities of thoracic aortic branches	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital transverse mandibular hyperplasia	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Right descending aorta	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Branchiooculofacial syndrome	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Capillary malformation	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Left dominant coronary system	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital malformation of posterior pituitary	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of parathyroid glands	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Meningoencephalocele	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Distichiasis	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Epidermodysplasia verruciformis	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Netherton's syndrome	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Lack of ossification of mandible	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Congenital transposition of azygos vein	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital portal-systemic shunt	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Autosomal dominant ichthyosis	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Common arterial trunk and widely separate origin of pulmonary arteries	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	4
Total anomalous pulmonary venous connection to coronary sinus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Total anomalous pulmonary venous connection to hepatic vein	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Total anomalous pulmonary venous connection to right atrium	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Total anomalous pulmonary venous connection to superior vena cava	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Localized congenital cutis laxa	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Double aortic arch	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital oculocutaneous hypopigmentation	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Vascular malformation of the nervous system	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Major systemic to pulmonary collateral artery with absent pulmonary arteries proximal to hilar bifurcation	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Double aortic arch with left arch dominant	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Anomalous course of coronary artery through infundibular septum	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Incomplete ossification of vomer	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Congenital anomaly of skin	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Generalized congenital intestinal dysmotility	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital malformation syndromes affecting facial appearance	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Cutaneous lesion resulting from spina bifida	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Anomalous termination of right pulmonary vein	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Infracardiac location of anomalous pulmonary venous connection with two descending veins	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Anonychia	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Double aortic arch with right arch dominant	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Overriding aorta	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of cardiovascular system	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Lamellar ichthyosis	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Congenital anomaly of exoccipital bone	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Balanced coronary system	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Collaterals to pulmonary arteries	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Bilateral closed ductus arteriosus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital cyst of esophagus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Cutaneous lesion resulting from spinal dysraphism	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital macrognathism	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital abnormality of thoracic aorta and pulmonary arteries	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Anomalous pulmonary venous connection of mixed type with one pulmonary venous confluence	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Anomalous intramural course of proximal portion of coronary artery above aortic sinus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Embryonal rest AND/OR persistent embryonic structure	Is a	False	Developmental anomaly	Inferred relationship	Existential restriction modifier
Seckel syndrome	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Salmon patch nevus	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Systemic to pulmonary collateral artery contributing to dual lung supply	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital anomaly of squamosal bone	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Congenital anomaly of the thyroid gland	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Anomalous course of coronary artery posterior to pulmonary trunk	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	1
Congenital coronary artery calcification	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Keratitis ichthyosis and deafness syndrome	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2
Vascular compression of esophagus by aberrant artery	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	4
Neurofibromatosis type 1	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	3
Persistent left superior vena cava	Associated morphology	False	Developmental anomaly	Inferred relationship	Existential restriction modifier	2

Start Previous Page 24 of 75 Next End

This concept is not in any reference sets

Back to Start

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