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1137472008: Neurodevelopmental delay (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Aug 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4526080011 Neurodevelopmental delay (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4526081010 Neurodevelopmental delay en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

124 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neurodevelopmental delay (disorder) Is a Developmental delay true Inferred relationship Some
Neurodevelopmental delay (disorder) Is a Neurodevelopmental disorder true Inferred relationship Some
Neurodevelopmental delay (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
SMARCA2-related blepharophimosis, intellectual disability syndrome Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Hereditary persistence of fetal hemoglobin, intellectual disability syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Hao Fountain syndrome Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Intellectual disability, severe speech delay, mild dysmorphism syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Mesomelic dysplasia, digital anomalies, intellectual disability syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Solute carrier family 12 member 2-related developmental delay, intellectual disability, sensorineural deafness syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Cyclin-dependent kinase-like 5 developmental and epileptic encephalopathy (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Neuronal ceroid lipofuscinosis type 2 Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Intellectual disability, speech delay, dysmorphic features, T cell abnormalities syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some
Developmental delay, language impairment, dopa responsive dystonia, parkinsonism syndrome (disorder) Is a True Neurodevelopmental delay (disorder) Inferred relationship Some

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