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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
82870011 Morphologic abnormality en Synonym Inactive Only initial character case insensitive SNOMED CT core module
82871010 Morphologic abnormality, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
82872015 Morphologic alteration, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
82873013 Morphologic change, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
82874019 Abnormal tissue appearance, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
82877014 Abnormal tissue appearance en Synonym Active Entire term case insensitive SNOMED CT core module
82878016 Abnormal appearance, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
198205018 Lesion en Synonym Inactive Only initial character 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
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital abnormality of uterus affecting obstetric care Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Horizontal orbital dystopia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Major systemic to pulmonary collateral artery with absent pulmonary arteries proximal to hilar bifurcation Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Major systemic to pulmonary collateral artery with absent pulmonary arteries proximal to hilar bifurcation Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Early onset myopathy with fatal cardiomyopathy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pericarditis secondary to Mulibrey nanism Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Developmental anomaly of odontoid process of axis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Autosomal dominant osteopetrosis type 2 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Leprechaunism syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Familial omphalocele syndrome with facial dysmorphism Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Ectodermal dysplasia with tooth-sweating defect Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
X-linked myopathy with excessive autophagy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Orbital separation diminished Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Uterus acollis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Platypellic pelvis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of atria and atrial septum Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of upper alimentary tract Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of renal pelvis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Axillary freckling due to neurofibromatosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Axillary freckling due to neurofibromatosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Mondini defect Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Tel Hashomer camptodactyly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Tel Hashomer camptodactyly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Aortic orifice left side by side with respect to pulmonary orifice Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta, hypoplastic type with microdontia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pleuropericardial cyst Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 5
Esophageal atresia, stenosis and fistula Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of maxilla Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectopic cilia of eyelid Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of aortic arch Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Macrophthalmos Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Bethlem myopathy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Embryopathy caused by phenobarbital Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of vitreous humor Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Major systemic to pulmonary collateral artery supplying part of right lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Major systemic to pulmonary collateral artery supplying part of right lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Ruvalcaba syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Ruvalcaba syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Blue sclera Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Caudal appendage deafness syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital dysplasia of left lobe of lung co-occurrent with congenital vascular malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Gorlin-Chaudhry-Moss syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Bilobed right lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Nevus anemicus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Levy-Hollister syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Potter sequence cleft lip and palate cardiopathy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Potter sequence cleft lip and palate cardiopathy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Isolation of subclavian artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Multiple malformation syndrome with facial-limb defects as major feature Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Multiple malformation syndrome with facial-limb defects as major feature Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Undescended testes - bilateral Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Pre-eruptive color change of tooth Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Oro-facial digital syndrome type 8 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Oro-facial digital syndrome type 8 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Oro-facial digital syndrome type 8 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Fronto-frontal dysostosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 34 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Autosomal recessive muscular dystrophy with gene located at 15q Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Lateral accessory root canals Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Lack of ossification of radius Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Hologastroschisis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of aortic arch AND/OR descending aorta Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital iodine deficiency syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Auricular abnormality, cleft lip, ocular abnormality syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital abnormality of ventricles and ventricular septum Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect - ventricular component under inferior bridging leaflet Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Multiple benign annular creases of extremities Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Absent thumb with short stature and immunodeficiency syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of pericardium Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Supramitral left atrial ring Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of lacrimal drainage system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Vertical orbital dystopia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital nuclear ophthalmoplegia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of nasal septum Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Systemic to pulmonary collateral artery from left brachiocephalic artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery from left brachiocephalic artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Overgrowth of upper limb Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Overgrowth of upper limb Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital vascular malformation of orbit Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Treacher Collins syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of hepatic vein Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of lower limb Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Corneal size and shape anomalies Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Vascular compression of esophagus by aberrant artery Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Multiple café-au-lait macules due to neurofibromatosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Multiple café-au-lait macules due to neurofibromatosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Reduction anomaly of hypothalamus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Reduction anomaly of hypothalamus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Tracheal origin of right upper lobe bronchus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Tracheal origin of right upper lobe bronchus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Alstrom syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Genetic defect of hair shaft Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Uterus cordiformis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1

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