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128305008: Abnormally opaque 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
206589016 Opacity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732282015 Abnormally opaque structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2764346010 Abnormally opaque structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206589016 Opacity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
206589016 Opacity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732282015 Abnormally opaque structure (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
732282015 Abnormally opaque structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2764346010 Abnormally opaque structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2764346010 Abnormally opaque structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
196261000077119 opacité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
196261000077119 opacité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Opacity Is a Degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Opacity Is a Lesion of degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital sclerocornea Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
opacité radiologique Associated morphology False Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Radiographic radiopacity of tooth Associated morphology False Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Opacity of bilateral lungs on plain chest X-ray (finding) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Grayson Wilbrandt dystrophy of cornea (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Adherent leukoma of left eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 5
Adherent leukoma of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 9
Adherent leukoma of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 7
Adherent leukoma of right eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 5
Vitreous opacity of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Vitreous opacity of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Vitreous opacity of right eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Opacity of cornea of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Opacity of cornea of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Opacity of cornea of left eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Opacity of cornea of right eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Vitreous opacity of left eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Thygeson superficial punctate keratitis (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology False Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Intellectual disability-cataracts-calcified pinnae-myopathy syndrome is a rare, genetic intellectual disability syndrome characterized by macrocephaly, hypotonia, dysmorphic facial features (wide forehead, ptosis, downslanting palpebral fissures, enlarged and calcified external ears, large jaw), sparse body hair, tall stature, and intellectual disability. Hearing loss, insulin-resistant diabetes, and progressive distal muscle wasting (leading to joint contractures) have also been reported in adulthood. Rare manifestations include behavioral abnormalities (aggression and restlessness), hypothyroidism, cerebral calcification, ataxia, and peripheral neuropathy. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Bilateral eye brunescent cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Bilateral eye brunescent cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic disease characterised by mild intellectual deficit, congenital cataract, progressive sensorineural hearing impairment, ataxia, peripheral neuropathy, and short stature. There have been no further descriptions in the literature since 1991. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cortical age-related cataract of right eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract with deafness and hypogonadism syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract of posterior subcapsule of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract of posterior subcapsule of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare syndromic endocrine disease characterized by the association of hypergonadotropic hypogonadism and cataracts with onset during adolescence. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Posterior subcapsular polar senile cataract of right eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract glaucoma syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract glaucoma syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cataract-hypertrichosis-intellectual disability syndrome is characterised by congenital cataract, generalised hypertrichosis and intellectual deficit. It has been described in two Egyptian siblings born to consanguineous parents. It is transmitted as an autosomal recessive trait. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cataract, congenital heart disease, neural tube defect syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 4
Zonular nonsenile cataract (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
MEDNIK-Syndrom Associated morphology False Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital subcapsular cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract of left eye due to and following trauma Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
This syndrome is characterized by the association of intellectual deficit, congenital cataract, and hypogonadotropic hypogonadism. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant optic atrophy and cataract (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract of right eye due to and following trauma Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile and/or juvenile cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Crome syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital cataract of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cataract ichthyosis syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract and microcornea syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Punctate age-related cataract (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Warburg micro syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cataract of posterior subcapsule of right eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Absence deformity of leg and congenital cataract syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anterior subcapsular polar cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract, hearing loss, severe developmental delay syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Cortical age-related cataract of left eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract due to pseudohypoparathyroidism Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract-intellectual disability-anal atresia-urinary defects syndrome is characterised by congenital cataracts with squint, intellectual deficit, anomalies of the genitourinary tract (rectovesical fistula, micropenis, undescended testis, and hypospadias), imperforate anus and other anomalies. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Brunescent cataract of right eye (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cochleosaccular degeneration and cataract syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Brunescent cataract of left eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 4
Cataract-aberrant oral frenula-growth delay syndrome is characterized by cataracts and short stature associated with variable anomalies, including aberrant oral frenula, a characteristic facial appearance (posteriorly angulated ears, upslanting palpebral fissures, small nose, ptosis and epicanthal folds) cavernous hemangiomas and hernias. It has been described in a mother and her two children. It is transmitted as an autosomal dominant trait. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital combined form cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Bilateral posterior subcapsular polar senile cataract of eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Bilateral posterior subcapsular polar senile cataract of eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Coronary age-related cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract of right eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Posterior subcapsular polar senile cataract of left eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract of left eye due to diabetes mellitus (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract of left eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Nathalie syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Bilateral posterior capsule opacification (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Bilateral posterior capsule opacification (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Diabetic cataract of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Diabetic cataract of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Right posterior capsule opacification not obscuring vision (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic central nervous system malformation syndrome characterized by bilateral congenital cataracts and severe hemorrhagic destruction of the brain parenchyma with associated massive cystic degeneration, enlarged ventricles and subependymal calcification. Patients typically present generalized spasticity, increased deep tendon reflexes and seizures. Hepatomegaly and renal anomalies have also been reported. Caused by homozygous mutation in the JAM3 gene on chromosome 11q25. Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Bilateral after-cataract not obscuring vision Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Bilateral after-cataract not obscuring vision Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cortical nonsenile cataract (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Presenile cataract of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Presenile cataract of bilateral eyes Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cortical age-related cataract of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cortical age-related cataract of bilateral eyes (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract of posterior subcapsule of left eye Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Foveal hypoplasia with presenile cataract syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Cataract of right eye due to diabetes mellitus Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Juvenile cataract, microcornea, renal glucosuria syndrome Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital posterior subcapsular polar cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypermature senile cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary cataract Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Left posterior capsule opacification not obscuring vision (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Cataract due to idiopathic hypoparathyroidism (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperferritinemia cataract syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital polar cataract (disorder) Associated morphology True Opacity Inferred relationship Existential restriction modifier (core metadata concept) 1

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