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49755003: Morphologically abnormal structure (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
82877014 Abnormal tissue appearance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
495494014 Morphologically abnormal structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
787468010 Morphologically abnormal structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3371000077116 structure anormale sur le plan morphologique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5223 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
Juvenile osteochondrosis of left second metatarsal Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Juvenile osteochondrosis of left tarsus Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Juvenile osteochondrosis of right tarsus (disorder) Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Juvenile osteochondrosis of bilateral tarsals (disorder) Associated morphology True Morphologically abnormal structure Inferred relationship Some 4
Tubal-cornual placenta Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Enamel spur Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Dieulafoy's vascular malformation Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Abnormal mature chorion Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Defect of vertebral segmentation Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Placenta membranacea Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Mature abnormal placenta Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Annular placenta Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Juvenile osteochondrosis of tibial tubercle (disorder) Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Blighted ovum Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Tenney changes of placenta Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Carneous mole Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Choriovitelline placenta Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Morbidly adherent placenta (disorder) Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Adherent placenta Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Mesio-occlusion of teeth Associated morphology False Morphologically abnormal structure Inferred relationship Some 3
Vertical overbite Associated morphology False Morphologically abnormal structure Inferred relationship Some 3
Anomaly of dental arch (disorder) Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Morbidly adherent placenta in which the chorionic villi invade through the myometrium. Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Dysmorphic sialidosis, congenital form Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Disto-occlusion of teeth Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Midline deviation of dental arch Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Class III buccal segment relationship - half unit Associated morphology False Morphologically abnormal structure Inferred relationship Some 3
Lateral openbite Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Lateral openbite - right Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Lateral openbite - left Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Abnormal placenta affecting management of mother Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Right posterior open bite Associated morphology False Morphologically abnormal structure Inferred relationship Some 2
Anomaly of interarch distance Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
A single anterior tooth pair is in crossbite and is also impinging on the soft tissue, resulting in destruction of the oral mucosa adjacent to one or both teeth involved. Associated morphology False Morphologically abnormal structure Inferred relationship Some 3
Juvenile osteochondrosis of lower ulna Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Juvenile osteochondrosis of primary patellar center Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Morbidly adherent placenta in which the chorionic villi attach to the myometrium, rather than being restricted to the decidua basalis. Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Juvenile osteochondrosis of head of metacarpals Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Juvenile osteochondrosis of hand Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Placenta accreta without hemorrhage Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Juvenile osteochondrosis of upper extremity Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Morbidly adherent placenta in which the chorionic villi invade into the myometrium. Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Placenta reflexa Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Immature abnormal placenta Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Postmature abnormal placenta Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Placenta multipartita Associated morphology False Morphologically abnormal structure Inferred relationship Some 1
Pendred's syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Placenta circumvallata Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Associated morphology True Morphologically abnormal structure Inferred relationship Some 5
Microcephaly-cervical spine fusion anomalies syndrome is characterized by microcephaly, facial dysmorphism (beaked nose, low-set ears, downslanting palpebral fissures, micrognathia), mild intellectual deficit, short stature, and cervical spine fusion anomalies producing spinal cord compression. It has been described in two brothers born to consanguineous parents. Transmission is likely to be autosomal recessive. Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Microcephaly with simplified gyral pattern Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
A rare syndrome described and characterized by prenatal onset of growth deficiency, microcephaly, hypoplastic genitalia, and birth onset of convulsions. Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
A rare syndromic intellectual deficiency characterized by psychomotor delay, severe progressive spastic quadriplegia, microcephaly, and a Hallermann-Streiff-like phenotype including absence of eyebrows and eyelashes, glaucoma, and small, beaked nose. Structural central nervous system abnormalities (cervical spinal cyst, occipital cranium bifidum occulatum) were additional findings. There have been no further descriptions in the literature since 1974. Associated morphology True Morphologically abnormal structure Inferred relationship Some 6
Caudal regression syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Curry-Hall syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 5
Caudal regression syndrome Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
A rare chromosomal anomaly syndrome, resulting from the partial deletion of the short arm of chromosome X, principally characterized by classical Norrie disease (bilateral, severe retinal malformations and opacity of the lens leading to congenital blindness, on occasion associated with progressive sensorineural deafness and intellectual disability), microcephaly, hypotonia, psychomotor and growth delay, moderate to severe mental handicap and disruptive behavior. Clinical phenotype is highly variable and immunodeficiency, epilepsy and hypogonadism have also been reported. Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
16p11.2-p12.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism. Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Congenital anomaly of blood vessel of spine (disorder) Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
A lysosomal storage disease with characteristics of coarse facial features, macular cherry red spot, and dysostosis multiplex. Clinical presentation can be heterogeneous ranging from a severe, early-onset, rapidly progressive infantile form to late onset, slowly progressive juvenile/adult form. Associated morphology True Morphologically abnormal structure Inferred relationship Some 3
Tetrasomy X is a sex chromosome anomaly caused by the presence of two extra X chromosomes in females (48,XXXX instead of 46,XX). Prevalence is unknown but only around 40 cases have been reported in the literature so far. Tetrasomy X is associated with delayed speech, learning difficulties, developmental delay and facial dysmorphism. Although disease severity is variable, the learning difficulties and developmental delay are generally mild to moderate. Commonly associated facial features include hypertelorism, upslanting palpebral fissures, epicanthal folds and a flat nasal bridge. Other anomalies may include dental abnormalities, hypotonia and joint laxity, radioulnar synostosis, heart defects, hip dysplasia, and ovarian dysfunction. An increased susceptibility to infections during childhood has also been reported. Tetrasomy X is generally thought to arise as a result of successive maternal nondisjunction during meiosis. Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
A disorder defining by the association of Perineal hemangioma, External genitalia malformations, Lipomyelomeningocele, Vesicorenal abnormalities, Imperforate anus, and Skin tag. Eleven cases have been reported. Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
A rare genetic disease characterized by patients presenting with a multitude of clinical features of Proteus syndrome without meeting the diagnostic criteria for the disease. Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Fibrolipoma of filum terminale Associated morphology True Morphologically abnormal structure Inferred relationship Some 2
Carrier of Becker muscular dystrophy (finding) Associated morphology True Morphologically abnormal structure Inferred relationship Some 1
Correction of congenital cardiovascular deformity (procedure) Direct morphology True Morphologically abnormal structure Inferred relationship Some 1
Correction of clubfoot (procedure) Direct morphology True Morphologically abnormal structure Inferred relationship Some 1
Correction of congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Intra-articular soft tissue procedure for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Extra-articular soft tissue procedure for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Osteotomy of ilium for correction of congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Femoral osteotomy for correction of congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Pelvic osteotomy for congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Salter osteotomy for congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Chiari osteotomy for congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Colonna osteotomy for congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Shelf procedure for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Excision of anlage of fibula Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Excision of anlage of tibia Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Centralization tarsus correction Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
ostéoplastie de retournement de la cheville Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Gruca tibial bifurcation procedure Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Creation of tibiofibular synostosis Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Correction of upper limb congenital ring constriction band Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Soft tissue procedure for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Excision of limbus for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 4
Adductor tenotomy for congenital dislocation of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 4
Triple pelvic osteotomy for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Correction of tibial pseudoarthrosis by excision and bone lengthening Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Correction of tibial pseudoarthrosis by free fibula graft Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Correction of tibial pseudoarthrosis by DCIA (deep circumflex iliac artery) bone flap Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Correction of obstetric palsy Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Primary osteotomy of pelvis for correction of congenital deformity of hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
arthroplastie secondaire de la hanche pour correction d'une malformation congénitale Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Proximal femoral osteotomy for correction of congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Pelvic osteotomy for congenital dislocation of the hip Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Repair of congenital pseudoarthrosis of tibia Direct morphology False Morphologically abnormal structure Inferred relationship Some 2
Correction of congenital deformity of upper limb Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Correction of congenital deformity of shoulder or upper arm Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
L'Episcopo operation for obstetric palsy (procedure) Direct morphology False Morphologically abnormal structure Inferred relationship Some 1
Zachary operation for obstetric palsy (procedure) Direct morphology False Morphologically abnormal structure Inferred relationship Some 1

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