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1217371005: Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Apr 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5036032016 Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5036033014 Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5036034015 SYT1-related neurodevelopmental disorder en Synonym Active Entire term case sensitive SNOMED CT core module
5036035019 Synaptotagmin 1-related neurodevelopmental disorder en Synonym Active Entire term case insensitive SNOMED CT core module
5036036018 Baker Gordon syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Global developmental delay true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Decreased muscle tone true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Movement disorder true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Is a Disorder of skeletal muscle true Inferred relationship Existential restriction modifier
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Interprets Movement true Inferred relationship Existential restriction modifier 5
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 3
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 4
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Interprets Muscle tone true Inferred relationship Existential restriction modifier 2
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 2
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Finding site Structure of visual system true Inferred relationship Existential restriction modifier 1
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 6
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 6
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 7
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 7

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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