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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
Ectopic thyroid tissue Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dermatoleukodystrophy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Ventricular imbalance Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Bohring Opitz syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Bohring Opitz syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Zebra body myopathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Right ventricular outflow tract absent Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Sotos' syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital malformation syndromes affecting facial appearance Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital heart disease Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dumbbell ossification of centrum of thoracic vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Limb mammary syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Ectopic ureterocele Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Vascular malformation of inner ear Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Acro-dermato-ungual-lacrimal-tooth syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital abnormality of atrial septum Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Myopathy with abnormality of histochemical fiber type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital hereditary muscular dystrophy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Juberg Hayward syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Juberg Hayward syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Juberg Hayward syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Endocrine-cerebro-osteodysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Endocrine-cerebro-osteodysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Mirror imaged atria Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Oro-facial digital syndrome type 11 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Oro-facial digital syndrome type 11 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 5
Oro-facial digital syndrome type 11 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Oro-facial digital syndrome type 11 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital abnormality of great veins and coronary sinus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital abnormality of great veins and coronary sinus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Isolation of brachiocephalic trunk Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of parietal bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Glossopalatine ankylosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Glossopalatine ankylosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Glossopalatine ankylosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Hepatic fibrosis, renal cyst, intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dolichopellic pelvis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Facio-auriculo-vertebral spectrum Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Systemic to pulmonary collateral artery from right carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Systemic to pulmonary collateral artery from right carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital protrusion of tongue Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Trabecular dysgenesis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
False anodontia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Abnormal plantar creases Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Abnormal plantar creases Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Osteopetrosis - delayed type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Myopathy with tubular aggregates Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with tooth-nail defects Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital trigger thumb Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Short stature with valvular heart disease and characteristic facies syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Solid rudimentary uterus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Port-wine stain of skin Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pulmonary hypertension in neurofibromatosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pulmonary hypertension in neurofibromatosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Spina bifida of dorsal region Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Lumbar myelocystocele Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital malformation of the respiratory system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Atrial septal defect through coronary sinus orifice Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Intellectual disability, balding, patella luxation, acromicria syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Floppy infant syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation through left septal commissure Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Localized congenital cutis laxa Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Primary congenital bronchomalacia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Trichomegaly with retina pigmentary degeneration and dwarfism syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of peripheral nerve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
X-linked intellectual disability Seemanova type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Interruption of coronary artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Solitary median maxillary central incisor syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cardiac anomaly and heterotaxy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Juxtaposed atrial appendage Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of optic nerve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Interruption of aortic arch between subclavian artery and common carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Trichorhinophalangeal dysplasia type I Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Trichorhinophalangeal dysplasia type I Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Trifid kidney Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pelvis justo major Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Multiple malformation syndrome, small stature, without skeletal dysplasia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of cornea Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cutis laxa, recessive, type I Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Major systemic to pulmonary collateral artery supplying entire right lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Major systemic to pulmonary collateral artery supplying entire right lung Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Werner syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of right atrioventricular valve leaflet in double inlet ventricle Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Oto-palato-digital syndrome, type II Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of great vessel Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Double uterus, hemivagina, renal agenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Double uterus, hemivagina, renal agenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cyclopia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Abnormality of right superior vena cava Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dumbbell-shaped cartilaginous centrum of cervical vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Holoprosencephaly sequence Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
46,XX disorder of sex development with skeletal anomalies syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
46,XX disorder of sex development with skeletal anomalies syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of anterior pituitary Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital female urogenital anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1

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