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21031007: Infratentorial brain structure (body structure)


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
35352012 Infratentorial brain en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
480906012 Infratentorial brain structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
750281010 Infratentorial brain structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


622 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infratentorial brain structure Is a Brain part false Inferred relationship Some
Infratentorial brain structure partie de Entire brain false Additional relationship Some
Infratentorial brain structure Is a Brain region true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Cerebellar structure Is a False Infratentorial brain structure Inferred relationship Some
Infratentorial brain part (body structure) Is a True Infratentorial brain structure Inferred relationship Some
Entire infratentorial brain Is a True Infratentorial brain structure Inferred relationship Some
Exploratory craniotomy, infratentorial Procedure site False Infratentorial brain structure Inferred relationship Some 1
Craniectomy for excision of meningioma, infratentorial Procedure site False Infratentorial brain structure Inferred relationship Some
Neoplasm of uncertain or unknown behaviour of brain, infratentorial Finding site False Infratentorial brain structure Inferred relationship Some 1
Craniectomy for excision of meningioma, infratentorial Procedure site - Direct (attribute) True Infratentorial brain structure Inferred relationship Some 2
Neoplasm of uncertain or unknown behaviour of brain, infratentorial Finding site True Infratentorial brain structure Inferred relationship Some 1
Excision of bone of cranium and excision of infratentorial neoplasm of brain (procedure) Procedure site - Direct (attribute) True Infratentorial brain structure Inferred relationship Some 2
Dandy-Walker syndrome Finding site True Infratentorial brain structure Inferred relationship Some 4
Cystic malformation of posterior fossa (disorder) Finding site False Infratentorial brain structure Inferred relationship Some 2
Dandy-Walker syndrome with spina bifida Finding site False Infratentorial brain structure Inferred relationship Some 4
Posterior fossa arachnoid cyst (disorder) Finding site False Infratentorial brain structure Inferred relationship Some 4
Persistent Blake's pouch cyst Finding site False Infratentorial brain structure Inferred relationship Some 2
Dandy-Walker syndrome with spina bifida Finding site True Infratentorial brain structure Inferred relationship Some 6
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. Finding site True Infratentorial brain structure Inferred relationship Some 8
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. Finding site False Infratentorial brain structure Inferred relationship Some 15
A rare central nervous system malformation characterized by severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead), and brain imaging abnormalities such as Dandy-Walker malformation, and iron deposition. Finding site False Infratentorial brain structure Inferred relationship Some 6
A rare central nervous system malformation characterized by severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead), and brain imaging abnormalities such as Dandy-Walker malformation, and iron deposition. Finding site False Infratentorial brain structure Inferred relationship Some 9
A rare malformation disorder characterized by sagittal craniosynostosis, Dandy-Walker malformation, hydrocephalus, craniofacial dysmorphism (including dolichocephaly, hypertelorism, micrognathia, positional ear deformity) and variable developmental delay. Finding site False Infratentorial brain structure Inferred relationship Some 10
A rare malformation disorder characterized by sagittal craniosynostosis, Dandy-Walker malformation, hydrocephalus, craniofacial dysmorphism (including dolichocephaly, hypertelorism, micrognathia, positional ear deformity) and variable developmental delay. Finding site False Infratentorial brain structure Inferred relationship Some 7
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. Finding site False Infratentorial brain structure Inferred relationship Some 11
A rare neurologic disease characterized by bilateral cataract, Dandy-Walker malformation, and childhood onset of distal spinal muscular atrophy. Patients present with progressively deteriorating symmetrical distal muscle weakness and atrophy of the lower limbs (and, to a much lesser degree, also the upper limbs) and decreased tendon reflexes in the lower and upper limbs. Finding site False Infratentorial brain structure Inferred relationship Some 8
A rare neurologic disease characterized by bilateral cataract, Dandy-Walker malformation, and childhood onset of distal spinal muscular atrophy. Patients present with progressively deteriorating symmetrical distal muscle weakness and atrophy of the lower limbs (and, to a much lesser degree, also the upper limbs) and decreased tendon reflexes in the lower and upper limbs. Finding site False Infratentorial brain structure Inferred relationship Some 5
A rare multiple congenital anomalies/dysmorphic syndrome characterized by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. Finding site False Infratentorial brain structure Inferred relationship Some 10
A syndromic disorder with, as a major feature, the association between Dandy-Walker malformation and postaxial polydactyly. The Dandy-Walker malformation has a variable expression and is characterized by a posterior fossa cyst communicating with the fourth ventricle, the partial or complete absence of the cerebellar vermis, and facultative hydrocephalus. Postaxial polydactyly includes tetramelic postaxial polydactyly of hands and feet with possible enlargement of the fifth metacarpal and metatarsal bones, as well as bifid fifth metacarpals. Finding site False Infratentorial brain structure Inferred relationship Some 6
A syndromic disorder with, as a major feature, the association between Dandy-Walker malformation and postaxial polydactyly. The Dandy-Walker malformation has a variable expression and is characterized by a posterior fossa cyst communicating with the fourth ventricle, the partial or complete absence of the cerebellar vermis, and facultative hydrocephalus. Postaxial polydactyly includes tetramelic postaxial polydactyly of hands and feet with possible enlargement of the fifth metacarpal and metatarsal bones, as well as bifid fifth metacarpals. Finding site False Infratentorial brain structure Inferred relationship Some 5
A rare multiple congenital anomalies/dysmorphic syndrome characterized by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. Finding site False Infratentorial brain structure Inferred relationship Some 7
Posterior fossa arachnoid cyst (disorder) Finding site True Infratentorial brain structure Inferred relationship Some 1
Persistent Blake's pouch cyst Finding site True Infratentorial brain structure Inferred relationship Some 1
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. Finding site True Infratentorial brain structure Inferred relationship Some 6
Cystic malformation of posterior fossa (disorder) Finding site True Infratentorial brain structure Inferred relationship Some 1
Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome is a rare, hereditary, cerebral malformation with epilepsy syndrome characterized by severe global developmental delay with no ability to walk and no verbal language, intractable epilepsy, partial agenesis of the corpus callosum and cerebellar vermis hypoplasia with posterior fossa cysts. Finding site True Infratentorial brain structure Inferred relationship Some 2
A rare multiple congenital anomalies/dysmorphic syndrome characterized by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989. Finding site True Infratentorial brain structure Inferred relationship Some 6
A rare malformation disorder characterized by sagittal craniosynostosis, Dandy-Walker malformation, hydrocephalus, craniofacial dysmorphism (including dolichocephaly, hypertelorism, micrognathia, positional ear deformity) and variable developmental delay. Finding site True Infratentorial brain structure Inferred relationship Some 6
A rare neurologic disease characterized by bilateral cataract, Dandy-Walker malformation, and childhood onset of distal spinal muscular atrophy. Patients present with progressively deteriorating symmetrical distal muscle weakness and atrophy of the lower limbs (and, to a much lesser degree, also the upper limbs) and decreased tendon reflexes in the lower and upper limbs. Finding site True Infratentorial brain structure Inferred relationship Some 4
A rare central nervous system malformation characterized by severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead), and brain imaging abnormalities such as Dandy-Walker malformation, and iron deposition. Finding site True Infratentorial brain structure Inferred relationship Some 5
A syndromic disorder with, as a major feature, the association between Dandy-Walker malformation and postaxial polydactyly. The Dandy-Walker malformation has a variable expression and is characterized by a posterior fossa cyst communicating with the fourth ventricle, the partial or complete absence of the cerebellar vermis, and facultative hydrocephalus. Postaxial polydactyly includes tetramelic postaxial polydactyly of hands and feet with possible enlargement of the fifth metacarpal and metatarsal bones, as well as bifid fifth metacarpals. Finding site True Infratentorial brain structure Inferred relationship Some 4
Benign neoplasm of infratentorial brain (disorder) Finding site True Infratentorial brain structure Inferred relationship Some 1
Exploratory craniotomy, infratentorial Procedure site - Indirect (attribute) True Infratentorial brain structure Inferred relationship Some 2

Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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