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49755003: Morphologically abnormal structure (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
82877014 Abnormal tissue appearance en Synonym Active Entire term case insensitive SNOMED CT core module
495494014 Morphologically abnormal structure en Synonym Active Entire term case insensitive SNOMED CT core module
787468010 Morphologically abnormal structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

5006 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Morphologically abnormal structure Is a Body structure, altered from its original anatomical structure true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Ethmocephalus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Triplex ureter Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Simpson-Golabi-Behmel syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ulegyria Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Fetal captopril/enalapril syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Malalignment of aortic sinus in relation to pulmonary sinus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital leg length discrepancy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital articular rigidity with myopathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
X-linked muscular dystrophy with abnormal dystrophin Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Jawad syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 5
Jawad syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Moore-Federman syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Genodermatosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Endemic congenital iodine deficiency syndrome of myxedematous type Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Encephalo-ophthalmic dysplasia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Noonan's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Precocious exfoliation due to ectopic eruption of proximate tooth Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital cataracts, facial dysmorphism and neuropathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital cataracts, facial dysmorphism and neuropathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Meckel-Gruber syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
46,XY ovotesticular disorder of sex development Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Deep vein aplasia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Failure of differentiation of bones of lower limb Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Failure of differentiation of bones of lower limb Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital pulmonary alveolar capillary dysplasia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Port-wine stain with oculocutaneous melanosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Bronchopulmonary collateral artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Bronchopulmonary collateral artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of lacrimal bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cerebral-retinal arteriovenous aneurysm Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Transient infantile osteopetrosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Embryopathy caused by mycophenolate mofetil Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of male genital system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital heterochromia iridis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of oral mucosa Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of joint Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Autosomal recessive centronuclear myopathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Retroesophageal aortic arch Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital deformity of right upper limb Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cylindrical embryo Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Eccentric opening of aortic valve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ramos Arroyo syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of angle of anterior chamber of eye Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lethal multiple pterygium syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lethal multiple pterygium syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery from left carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery from left carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lobar holoprosencephaly Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Familial vesicoureteral reflux Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Karsch Neugebauer syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Duane's syndrome, type 3 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Duane's syndrome, type 3 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta - hypomaturation - recessive pigmented Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Craniofacial ulnar renal syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Female infertility due to structural congenital anomaly of cervix Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Infantile malignant osteopetrosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital polyneuropathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of relationship of cardiac component Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of centrum of sacral vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Trisomy 10p Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Trisomy 10p Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Upper limb defect with eye and ear abnormalities syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Upper limb defect with eye and ear abnormalities syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of the hematopoietic system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lymphedema hypoparathyroidism syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Eccentric opening of tricuspid aortic valve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of metatarsal bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
FG syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
FG syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Persistent vertical vein Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Persistent vertical vein Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Immotile cilia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Right ventricular outflow tract abnormality Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Simple ureterocele Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery contributing to dual lung supply Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Systemic to pulmonary collateral artery contributing to dual lung supply Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Developmental ovarian cyst Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital vascular malformation of lip Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Fetal or neonatal effect of maternal use of alcohol Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital deformity of left finger Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of cricoid cartilage Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Fetal carbamazepine syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ebstein's anomaly of left atrioventricular valve in functionally univentricular heart Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Ebstein's anomaly of left atrioventricular valve in functionally univentricular heart Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Persistent tunica vasculosa lentis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Persistent tunica vasculosa lentis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital trigger finger of right hand Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital blind loop syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dubin-Johnson syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of metacarpal bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Matthew Wood syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Matthew Wood syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Escobar syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital right vesicoureterorenal reflux Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2

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