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86765009: Mild intellectual disability (disorder)

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
143892017 Mild mental retardation (I.Q. 50-70) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
507246016 Mild mental retardation, IQ in range 50-70 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2975045012 Mild mental retardation (Intelligence Quotient 50-70) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643512010 Mild intellectual disability (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643513017 Mild intellectual disability en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3654174011 Mild intellectual development disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1858251000195119 disabilità intellettiva lieve it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
287261000172111 retard mental léger (Q.I. de 50 à 70) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1100961000241112 déficience intellectuelle légère fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1100971000241116 retard mental léger (quotient intellectuel de 50 à 70) fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
581881000274114 Leichte geistige Behinderung de Synonym (core metadata concept) Active Only initial character case insensitive (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
Mild intellectual disability (disorder) Is a Developmental academic disorder false Inferred relationship Some
Mild intellectual disability (disorder) Is a retard mental false Inferred relationship Some
Mild intellectual disability (disorder) Finding site Brain structure false Inferred relationship Some
Mild intellectual disability (disorder) Severity Mild false Inferred relationship Some
Mild intellectual disability (disorder) Is a Intellectual disability true Inferred relationship Some
Mild intellectual disability (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Mild intellectual disability (disorder) Interprets Intellectual ability true Inferred relationship Some 2
Mild intellectual disability (disorder) Has interpretation Impaired true Inferred relationship Some 2
Mild intellectual disability (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 3
Mild intellectual disability (disorder) Has interpretation Impaired true Inferred relationship Some 3
Inbound Relationships Type Active Source Characteristic Refinability Group
[X]Mild mental retardation with the statement of no, or minimal, impairment of behavior Is a False Mild intellectual disability (disorder) Inferred relationship Some
[X]Mild mental retardation, significant impairment of behavior requiring attention or treatment Is a False Mild intellectual disability (disorder) Inferred relationship Some
[X]Mild mental retardation, other impairments of behavior Is a False Mild intellectual disability (disorder) Inferred relationship Some
[X]Mild mental retardation without mention of impairment of behavior Is a False Mild intellectual disability (disorder) Inferred relationship Some
A rare, genetic, syndromic intellectual disability disorder characterized by congenital, persistent microcephaly, low birth weight, short stature, childhood-onset seizures, global development delay, mild intellectual disability, and adolescent or young adult-onset diabetes mellitus. Gait ataxia, skeletal abnormalities, dorsocervical fat pad, and infantile cirrhosis may also be associated. Brain morphology is typically normal, although delayed myelination and hypoplastic brainstem have been reported. Is a True Mild intellectual disability (disorder) Inferred relationship Some
2p21 microdeletion syndrome without cystinuria is a rare partial autosomal monosomy characterized by weak fetal movements, severe infantile hypotonia and feeding difficulties that spontaneously improve with time, urogenital abnormalities (hypospadias or hypoplastic labia majora), global development delay, mild intellectual disability and facial dysmorphism (dolichocephaly, frontal bossing, bilateral ptosis, midface retrusion, open mouth with tented upper lip vermilion). Affected individuals have borderline elevated serum lactate but no cystinuria. Is a True Mild intellectual disability (disorder) Inferred relationship Some

This concept is not in any reference sets

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