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1260143005: Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Dec 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5159439011 Megalencephaly, severe kyphoscoliosis, overgrowth syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159440013 Megalencephaly, severe kyphoscoliosis, overgrowth syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400416015 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by overgrowth and macrocephaly with megalencephaly apparent at birth, global developmental delay, intellectual disability, and dysmorphic facial features (including frontal bossing, long face, sparse eyebrows, hypertelorism, downslanting palpebral fissures, and prognathism). Patients may exhibit tall stature with dolichostenomelia, arachnodactyly, kyphoscoliosis, and joint laxity, as well as neurologic manifestations, such as hypotonia, gait ataxia, or seizures. Brain imaging may show increased white matter volume, thick corpus callosum, or small cerebellum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400417012 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by overgrowth and macrocephaly with megalencephaly apparent at birth, global developmental delay, intellectual disability, and dysmorphic facial features (including frontal bossing, long face, sparse eyebrows, hypertelorism, downslanting palpebral fissures, and prognathism). Patients may exhibit tall stature with dolichostenomelia, arachnodactyly, kyphoscoliosis, and joint laxity, as well as neurologic manifestations, such as hypotonia, gait ataxia, or seizures. Brain imaging may show increased white matter volume, thick corpus callosum, or small cerebellum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Intellectual disability true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Congenital macrocephaly (disorder) true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Global developmental delay true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Multiple malformation syndrome with early overgrowth true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Is a Macroencephaly true Inferred relationship Some
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 3
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Has interpretation Impaired true Inferred relationship Some 3
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 4
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Has interpretation Impaired true Inferred relationship Some 4
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Interprets Head circumference true Inferred relationship Some 5
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Has interpretation Above reference range true Inferred relationship Some 5
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Occurrence Congenital true Inferred relationship Some 1
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Finding site Cerebrum true Inferred relationship Some 1
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 1
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Occurrence Congenital true Inferred relationship Some 2
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Finding site Face structure true Inferred relationship Some 2
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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US English

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