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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
Fetal aminopterin syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Isomerism of atrial appendages Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Persistent urogenital sinus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Proximal penile hypospadias Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Nasofrontal encephalocele Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital bronchial stenosis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Okamoto syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Occult spinal dysraphism sequence Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Exaggerated cingulum of tooth Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of sclera Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Oral lymphangioma Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Holoprosencephaly with caudal dysgenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Status marmoratus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Status marmoratus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Disorder of sex development with intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Intellectual disability Birk-Barel type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
46,XY partial gonadal dysgenesis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital myopathy with fiber type disproportion Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Curly hair, ankyloblepharon, nail dysplasia syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Curly hair, ankyloblepharon, nail dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery from coronary artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery from coronary artery Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Systemic to pulmonary collateral artery from coronary artery Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Familial caudal dysgenesis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 5
Pilodental dysplasia, refractive errors syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Pilodental dysplasia, refractive errors syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Double ureter Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of thorax Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Warsaw breakage syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Right dominant coronary system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Delayed membranous cranial ossification Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Abnormal relationship of aortic orifice to pulmonary orifice Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of exoccipital bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Microcephaly, thin corpus callosum, intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lower moiety ureter of duplex kidney Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Jervell and Lange-Nielsen syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of upper limb Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of the urinary system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of organ of Corti Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of fallopian tubes Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Macrodontia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of rib Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Schwartz-Jampel syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Neurofibromatosis syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Neurofibromatosis syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Synchilia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital malformation of corpus callosum Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Synotus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Aortic orifice anterior with respect to pulmonary orifice Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital pulmonary venous atrium Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Arrhythmogenic right ventricular dysplasia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Anomalies of great veins Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Patent right ductus arteriosus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital ball and socket ankle Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Interrupted aortic arch Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Osteopetrosis - intermediate type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Maternal phenylketonuria fetal effect Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Dumbbell ossification of centrum of lumbar vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Acute respiratory distress in newborn with surfactant disorder Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of mitral subvalvular apparatus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of lower respiratory system Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Fetal misoprostol syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of pulmonary trunk Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ji muscular dystrophy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital bronchopulmonary foregut malformation Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Blepharonasofacial malformation syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
De Lange syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital athetosis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Meacham syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Meacham syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Meacham syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Biemond's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Isomerism of right atrial appendage Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Isomerism of right atrial appendage Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pena-Shokeir syndrome type I Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Benign Samaritan congenital myopathy Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Marfanoid habitus with autosomal recessive intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital ectodermal defect Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Nasopharyngeal encephalocele Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Sturge-Weber syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Sturge-Weber syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Sturge-Weber syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital anomaly of cervix Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Genetic disorder of surfactant dysfunction Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Horner's teeth Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cataract with aberrant oral frenula and growth delay syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital tracheomalacia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Deafness and intellectual disability Martin Probst type syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with ventricular component and shunting under connecting tongue with separate orifices Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital abnormality of salivary duct Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital myopathy with uniform fiber type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
X-linked intellectual disability Cabezas type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital malformation of uterus and cervix Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1

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