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1303868000: Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5308232015 Intermediate DEND syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5308233013 Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308234019 Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308236017 Intermediate DEND (developmental delay, epilepsy, neonatal diabetes) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5308235018 A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5308232015 Intermediate DEND syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5308233013 Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308234019 Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308236017 Intermediate DEND (developmental delay, epilepsy, neonatal diabetes) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5308235018 A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Is a Neonatal diabetes mellitus true Inferred relationship Existential restriction modifier (core metadata concept)
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Is a Developmental delay true Inferred relationship Existential restriction modifier (core metadata concept)
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Is a Neonatal metabolic disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Is a Neonatal disorder of endocrine system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Finding site Structure of endocrine system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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