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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


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 Mental retardation 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 Congenital dilatation 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 Congenital dilatation 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

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

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