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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 abnormality of vein Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Penoscrotal hypospadias Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Alacrima Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with hair-tooth-nail defects Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Biliary anomalies Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of supraoccipital bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Bilateral muscular infundibula Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia and sensorineural deafness syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital myopathy with myasthenic-like onset Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Mulibrey nanism syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Hemicentric lumbar centrum Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Carpenter Waziri syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Carpenter Waziri syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of ureter Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital partial portal-systemic shunt Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cutaneous lesion resulting from spinal dysraphism Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Syndromic X-linked intellectual disability type 11 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of abdomen Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Hall Riggs syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital anomaly of eyelid Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of sacral vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Lack of ossification of basioccipital bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of the urinary tract proper Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Venous remnant Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Widely spaced right coronary artery and left coronary artery orifices within single aortic sinus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Widely spaced right coronary artery and left coronary artery orifices within single aortic sinus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with sweating defect Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 5
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Trichothiodystrophy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Trichothiodystrophy Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Sacral spina bifida without hydrocephalus - open Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Congenital anomaly of fetus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ameloonychohypohidrotic syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Straddling tricuspid valve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Isomerism of left atrial appendage Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Isomerism of left atrial appendage Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of ocular adnexa Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Diffuse lymphatic malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Café-au-lait macules with temporal dysrhythmia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Café-au-lait macules with temporal dysrhythmia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Bicornuate uterus - baby delivered Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of oral cavity Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Aortic orifice anterior right with respect to pulmonary orifice Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Inclusion body myopathy 2 Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Beaked pelvis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of orbit proper Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Isolation of branch of aortic arch Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Camptodactyly with joint contracture and facial skeletal defect syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Camptodactyly with joint contracture and facial skeletal defect syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Pelviscapular dysplasia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Intracardiac location of anomalous pulmonary venous connection Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Regional odontodysplasia Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Uncombable hair syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Branchiootic syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Branchiootic syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Low anorectal malformation Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Brachytelephalangy, facial dysmorphism, Kallmann syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Brachytelephalangy, facial dysmorphism, Kallmann syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Abnormal atrial arrangement Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Cervical spina bifida with hydrocephalus - open Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital anomaly of nervous system of head/neck Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital deformity of left upper limb Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital maxillary asymmetry Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital abnormality of pulmonary valve cusp Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital urethral valve Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital subglottic web of larynx Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Shprintzen Goldberg craniosynostosis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Taurodontia with absent teeth and sparse hair syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 4
Congenital curly toes Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of descending thoracic aorta Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with acanthosis nigricans syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Interatrial communication through coronary sinus orifice Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Prader-Willi syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Lymphedema, atrial septal defect, facial changes syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Lack of ossification of talus Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of jaw Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Transitional vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Spina bifida of cervical region Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Nevus comedonicus Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Sinus pericranii Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Freeman-Sheldon syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Swan's syndrome II Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Port-wine stain associated with spinal dysraphism Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Port-wine stain associated with spinal dysraphism Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Congenital anomaly of squamosal bone Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Curry-Hall syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Marshall syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Hydatid cyst of Morgagni - female Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital deafness with labyrinthine aplasia, microtia and microdontia Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Persistent descending vein Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2
Persistent descending vein Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Congenital anomaly of broad ligament Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Toriello Carey syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 1
Hypohidrosis with neurolabyrinthitis Associated morphology True Morphologically abnormal structure Inferred relationship Existential restriction modifier 3
Uniatrial biventricular connection with absent right sided atrioventricular connection with straddling valve Associated morphology False Morphologically abnormal structure Inferred relationship Existential restriction modifier 2

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