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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
Congenital female urogenital anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Sex reversion, kidney, adrenal and lung dysgenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Sex reversion, kidney, adrenal and lung dysgenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Sex reversion, kidney, adrenal and lung dysgenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Sex reversion, kidney, adrenal and lung dysgenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Juberg Marsidi syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Wiedemann Steiner syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of head Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of presphenoid bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Cranio-orbito-ocular dysraphia syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of eye Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormal long growth of bile duct Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Undescended testicle Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Isotretinoin embryopathy-like syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Isotretinoin embryopathy-like syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Capillary-venous malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Capillary-venous malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Vascular compression of esophagus by aberrant right subclavian artery arising from descending aorta Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital corneal opacity interfering with vision Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Arachnodactyly with abnormal ossification and intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital abnormality of uterus in pregnancy, childbirth and the puerperium Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital asymmetry of jaw Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Orbital dystopia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of digestive tract Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of endocrine gland Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dento-oculocutaneous syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Plantarflexed cuboid Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Plantarflexed cuboid Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Overriding mitral valve Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of small intestine Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Femoral hypoplasia - unusual facies syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Anomalous coronary artery with acute angulation of less than 45 degrees relative to aorta Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Peters plus syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Distichiasis-lymphedema syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Straddling mitral valve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of intestinal tract Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pyknoachondrogenesis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia with alopecia and genital anomaly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Macropalpebral fissure Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Macropalpebral fissure Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of ear with impairment of hearing Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of dural sinus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Triple kidney with triple pelvis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Reduction deformities of brain Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cleft leaflet of tricuspid valve Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Diplomyelia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Diplomyelia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Embryofetopathy caused by indomethacin Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of lens Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cutis laxa, recessive, type II Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Gillespie syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Desmin-related myofibrillar myopathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of central nervous system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Spina bifida aperta of lumbar spine Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Major systemic to pulmonary collateral artery supplying entire left lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Major systemic to pulmonary collateral artery supplying entire left lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital tracheobronchomegaly Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital tracheobronchomegaly Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Specified anomalies of sclera Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of right atrioventricular valve papillary muscle in double inlet ventricle Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Thyroglossal duct anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cervical spina bifida with hydrocephalus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Reniform pelvis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital epiblepharon-inferior oblique syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital exotropia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Protrusion of tooth Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Hypoplastic enamel-onycholysis-hypohidrosis syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Brugsch's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cerebro-costo-mandibular syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Lowry MacLean syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Myotubular myopathy with type I atrophy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of abdominal wall Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
46,XX disorder of sex development with anorectal anomalies syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Right aortic arch branching pattern Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Merosin deficient congenital muscular dystrophy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Double eyebrow Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Double eyebrow Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Severe autosomal recessive muscular dystrophy of childhood - North African type Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital abnormality of left atrioventricular valve chordae tendinae in double inlet ventricle Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomalies of eyelid, lacrimal system and orbit Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital anomalies of eyelid, lacrimal system and orbit Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomalies of eyelid, lacrimal system and orbit Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of the thyroid gland Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Edinburgh malformation syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Imperforate left ventriculoarterial valve Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Oculofaciocardiodental syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Intracardiac location of anomalous pulmonary venous connection to coronary sinus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Venous-lymphatic malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Venous-lymphatic malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of pelvic bones Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Arachnodactyly and intellectual disability with facial dysmorphism syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Irido-corneal dysgenesis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2

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