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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 anomaly of iris Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pure gonadal dysgenesis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cerebral cortical dysgenesis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of liver Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of tympanic anulus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Borjeson-Forssman-Lehmann syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Myocardial bridge of coronary artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Acephalostomia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Separate hepatic vein and inferior vena cava connections to heart Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Aprosencephaly Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Embedded tooth Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of body cavity Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of thoracic vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of skeletal muscle Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Aortic orifice posterior left with respect to pulmonary orifice Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of tibia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Warburg syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cervical spina bifida without hydrocephalus - closed Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Thymic, renal, anal, lung dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Aqueduct of Sylvius anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Hydrolethalus syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by methimazole Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
X-linked intellectual disability Stevenson type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
X-linked intellectual disability Stevenson type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital developmental anomaly of cystic duct Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Charlie M syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Charlie M syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Charlie M syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Charlie M syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Kohlschutter's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Kohlschutter's syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Secondary congenital bronchomalacia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Spina bifida of lumbar region Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cervical thymic remnant Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Bicornuate uterus complicating antenatal care, baby not yet delivered Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pierre Robin sequence, congenital heart defect, talipes syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pentalogy of Cantrell Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lethal faciocardiomelic dysplasia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
McDonough syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ochoa syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Atresia and stenosis of large intestine, rectum and anal canal Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Marie Unna syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anosmia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ackerman syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Ackerman syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Crouzon syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Maxillonasal dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital myopathy with internal nuclei and atypical cores Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Usher syndrome type 2 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Fibrolipoma of filum terminale Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of cerebrovascular system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Duodenal web Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Duodenal web Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Absent blood vessel in umbilical cord Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Perodactylia of lesser toe Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anterior urethral valve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Acrosyndactyly of toe Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of pancreas Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of optic disc Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Grob's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Duane-radial ray syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of basioccipital bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Benign autosomal dominant osteopetrosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pallister-Hall syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Puerto Rican infant hypotonia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Puerto Rican infant hypotonia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Puerto Rican infant hypotonia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Hemimyelia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Lack of ossification of ulna Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Peg-shaped teeth Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital hypothyroidism without goiter Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Auriculo-condylar syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Auriculo-condylar syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Aganglionosis of large intestine Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Totally absent pericardium Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Cor triatriatum Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of finger Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Epispadias Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Epispadias Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Coronary orifice asymmetrical Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Coronary orifice asymmetrical Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of vomer Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cleft palate with short stature and vertebral anomaly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Lack of ossification of alisphenoid bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Fukuyama congenital muscular dystrophy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Transitional lumbosacral vertebra Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pseudoaminopterin syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pseudoaminopterin syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital malformation of clitoris Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of salivary gland Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of retina Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Acrorenoocular syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Acrorenoocular syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Acrorenoocular syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of tongue, mouth and pharynx Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of tongue, mouth and pharynx Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2

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