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716996008: Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308122015 Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308123013 L1 syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308124019 CRASH syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5155332010 Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5155333017 Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401436011 A rare, congenital X-linked developmental disorder characterized by hydrocephalus of varying degrees of severity, intellectual deficit, spasticity of the legs, and adducted thumbs. The syndrome represents a spectrum of disorders including: X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS), MASA syndrome, X-linked complicated hereditary spastic paraplegia type 1, and X-linked complicated corpus callosum agenesis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401437019 A rare, congenital X-linked developmental disorder characterised by hydrocephalus of varying degrees of severity, intellectual deficit, spasticity of the legs, and adducted thumbs. The syndrome represents a spectrum of disorders including: X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS), MASA syndrome, X-linked complicated hereditary spastic paraplegia type 1, and X-linked complicated corpus callosum agenesis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308121010 Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308121010 Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308122015 Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308122015 Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308123013 L1 syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308124019 CRASH syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5155332010 Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5155333017 Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3308125018 A mild to severe congenital X-linked developmental disorder with hydrocephalus of varying degrees of severity, intellectual deficit, spasticity of the legs, and adducted thumbs. Primarily affects males. Affected males have varying degrees of hydrocephalus ranging from subclinical to severe. Intellectual deficit ranges from mild to severe. Adducted thumbs are a characteristic feature of the syndrome, present in about 50% of cases. Caused by mutations in the L1CAM gene (Xq28) encoding the L1 cell adhesion molecule that is expressed mainly in the developing nervous system. Inherited in an X-linked manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401436011 A rare, congenital X-linked developmental disorder characterized by hydrocephalus of varying degrees of severity, intellectual deficit, spasticity of the legs, and adducted thumbs. The syndrome represents a spectrum of disorders including: X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS), MASA syndrome, X-linked complicated hereditary spastic paraplegia type 1, and X-linked complicated corpus callosum agenesis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401437019 A rare, congenital X-linked developmental disorder characterised by hydrocephalus of varying degrees of severity, intellectual deficit, spasticity of the legs, and adducted thumbs. The syndrome represents a spectrum of disorders including: X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS), MASA syndrome, X-linked complicated hereditary spastic paraplegia type 1, and X-linked complicated corpus callosum agenesis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3428081001000111 L1-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5477741000241119 syndrome d'hypoplasie du corps calleux et de retard mental avec pouces en adduction, spasticité et hydrocéphalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5477741000241119 syndrome d'hypoplasie du corps calleux et de retard mental avec pouces en adduction, spasticité et hydrocéphalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428081001000111 L1-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
L1 syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Is a retard mental false Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Is a Hypoplasia of corpus callosum true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
L1 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
L1 syndrome Finding site Corpus callosum structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
L1 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
L1 syndrome Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 2
L1 syndrome Finding site Structure of brain cerebrospinal fluid pathway (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
L1 syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
L1 syndrome Finding site Corpus callosum structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
L1 syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
L1 syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
L1 syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
L1 syndrome Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 1
L1 syndrome Finding site Structure of brain cerebrospinal fluid pathway (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
L1 syndrome Is a Congenital hydrocephalus true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Associated morphology Dilatation true Inferred relationship Existential restriction modifier (core metadata concept) 1
L1 syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
L1 syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3
L1 syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
L1 syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 4
L1 syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group
MASA syndrome Is a True L1 syndrome Inferred relationship Existential restriction modifier (core metadata concept)
X-linked complicated corpus callosum dysgenesis Is a True L1 syndrome Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

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

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