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49755003: Morphologically abnormal structure (morphologic abnormality)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
495494014 Morphologically abnormal structure en Synonym Active Case insensitive SNOMED CT core
787468010 Morphologically abnormal structure (morphologic abnormality) en Fully specified name Active Case insensitive SNOMED CT core
82877014 Abnormal tissue appearance en Synonym Active Case insensitive SNOMED CT core


4996 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Morphologically abnormal structure Is a Morphologically altered structure true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Blepharonasofacial malformation syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
De Lange syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital athetosis Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Meacham syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Meacham syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Meacham syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Biemond's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Isomerism of right atrial appendage Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Isomerism of right atrial appendage Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Pena-Shokeir syndrome type I Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Benign Samaritan congenital myopathy Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Marfanoid habitus with autosomal recessive intellectual disability syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital ectodermal defect Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Nasopharyngeal encephalocele Associated morphology False Morphologically abnormal structure Inferred relationship Some 4
Sturge-Weber syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Sturge-Weber syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Some 4
Sturge-Weber syndrome Associated morphology False Morphologically abnormal structure Inferred relationship Some 3
Congenital anomaly of cervix Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Genetic disorder of surfactant dysfunction Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Horner's teeth Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Wellesley Carman French syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Congenital tracheomalacia Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Deafness and intellectual disability Martin Probst type syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Atrioventricular septal defect with ventricular component and shunting under connecting tongue with separate orifices Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Congenital abnormality of salivary duct Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital myopathy with uniform fibre type Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
X-linked intellectual disability Cabezas type Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital anomaly of uterus and cervix Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital anomaly of uterus and cervix Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Congenital anomaly of aortic valve Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Eccentric opening of tricuspid pulmonary valve Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital anomaly of membranous labyrinth Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Structural anomaly of the cochlea and vestibular labyrinth Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Pseudocoarctation of aorta Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital uterine anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Lack of ossification of parietal bone Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Trisomy 17p Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Left dominant coronary system Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital anomaly of rectum Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Accessory tissue on aortic valve cusp Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Lack of ossification of femur Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Developmental malformation, deafness, dystonia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Char syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital iodine deficiency syndrome of neurological type Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Acromelic frontonasal dysplasia Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital hypothyroidism with ectopic thyroid Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Deafness craniofacial syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Inherited cutis laxa Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Velofacioskeletal syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Velofacioskeletal syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Multiple malformation syndrome, moderate short stature, facial Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behaviour syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Blunderbuss pelvis Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Pachydermoperiostosis of nail Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Pachydermoperiostosis of nail Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
X-linked hydrocephalus syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Osteopetrosis with renal tubular acidosis Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Dumbbell ossification of centrum of sacral vertebra Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Isolation of right common carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
LIG4 syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital supravalvular mitral stenosis Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Familial absence of villi Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Spina bifida occulta Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Fetal primidone syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital iris ectropion Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Hereditary myopathy limited to females Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Ectodermal dysplasia with hair-tooth-nail-sweating defect Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Posteromedial muscle band Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Lower limb malformation hypospadias syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Single coronary artery Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Splenoportal vascular anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Splenoportal vascular anomaly Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Phocomelia of upper limb Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Tricho-retino-dento-digital syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Acrocallosal syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Acrocallosal syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Congenital anomaly of pupil Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Angioma serpiginosum Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Umbilical vein varix Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Congenital anomaly of palatine bone Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Testicular dysgenesis syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Klippel's disease Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Interruption of aortic arch between left common carotid artery and right common carotid artery Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Congenital disorders of eye and eyelid movements Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Congenital bronchomalacia Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Spondyloepiphyseal dysplasia Cantu type Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Spondyloepiphyseal dysplasia Cantu type Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Congenital deafness Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Congenital anomaly of ear Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Coarctation of left pulmonary artery Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Malformation defect spectrum Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Abnormal attachment of tricuspid chordae tendinae Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Oral-facial-digital syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Oral-facial-digital syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Oral-facial-digital syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 5
Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1

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