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716996008: syndroom van hypoplasie van corpus callosum, verstandelijke beperking, geadduceerde digiti I, spasticiteit en hydrocefalie (aandoening)


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
6801101000146110 L1-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6801111000146112 L1CAM-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6941141000146113 syndroom van hypoplasie van corpus callosum, mentale retardatie, geadduceerde duimen, spasticiteit en hydrocefalie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6941161000146114 CRASH-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7719651000146115 syndroom van hypoplasie van corpus callosum, verstandelijke beperking, geadduceerde duimen, spasticiteit en hydrocefalie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7858701000146110 syndroom van hypoplasie van corpus callosum, verstandelijke handicap, geadduceerde duimen, spasticiteit en hydrocefalie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12020041000146111 syndroom van hypoplasie van corpus callosum, verstandelijke beperking, geadduceerde digiti I, spasticiteit en hydrocefalie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12208601000146115 syndroom van hypoplasie van corpus callosum, verstandelijke beperking, geadduceerde digiti I, spasticiteit en hydrocefalie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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


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 Some
L1 syndrome Is a mentale retardatie false Inferred relationship Some
L1 syndrome Is a X-linked hereditary disease false Inferred relationship Some
L1 syndrome Is a Hypoplasia of corpus callosum (disorder) true Inferred relationship Some
L1 syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
L1 syndrome Associated morphology Hypoplasia true Inferred relationship Some 2
L1 syndrome Occurrence Congenital true Inferred relationship Some 2
L1 syndrome Finding site Corpus callosum structure true Inferred relationship Some 2
L1 syndrome Occurrence Congenital false Inferred relationship Some 3
L1 syndrome Associated morphology congenitale dilatatie (afwijkende morfologie) false Inferred relationship Some 2
L1 syndrome Finding site Brain cerebrospinal fluid pathway false Inferred relationship Some 2
L1 syndrome Associated morphology Hypoplasia false Inferred relationship Some 3
L1 syndrome Finding site Corpus callosum structure false Inferred relationship Some 3
L1 syndrome Is a Intellectual disability true Inferred relationship Some
L1 syndrome Occurrence Congenital true Inferred relationship Some 1
L1 syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
L1 syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
L1 syndrome Associated morphology congenitale dilatatie (afwijkende morfologie) false Inferred relationship Some 1
L1 syndrome Finding site Brain cerebrospinal fluid pathway true Inferred relationship Some 1
L1 syndrome Is a Congenital hydrocephalus true Inferred relationship Some
L1 syndrome Associated morphology Dilatation true Inferred relationship Some 1
L1 syndrome Is a Developmental hereditary disorder true Inferred relationship Some
L1 syndrome Is a X-linked recessive hereditary disease true Inferred relationship Some
L1 syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 3
L1 syndrome Has interpretation Impaired true Inferred relationship Some 3
L1 syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 4
L1 syndrome Has interpretation Impaired true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group
MASA syndrome Is a True L1 syndrome Inferred relationship Some
X-linked complicated corpus callosum dysgenesis (disorder) Is a True L1 syndrome Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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