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770754006: 2p21 microdeletion syndrome without cystinuria (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3702465012 2p21 microdeletion syndrome without cystinuria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3702466013 2p21 microdeletion syndrome without cystinuria en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
2p21 microdeletion syndrome without cystinuria Finding site Chromosome pair 2 false Inferred relationship Existential restriction modifier 2
2p21 microdeletion syndrome without cystinuria Occurrence Congenital true Inferred relationship Existential restriction modifier 1
2p21 microdeletion syndrome without cystinuria Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 1
2p21 microdeletion syndrome without cystinuria Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
2p21 microdeletion syndrome without cystinuria Is a Deletion of part of short arm of chromosome 2 true Inferred relationship Existential restriction modifier
2p21 microdeletion syndrome without cystinuria Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
2p21 microdeletion syndrome without cystinuria Finding site Chromosome pair 2 true Inferred relationship Existential restriction modifier 1
2p21 microdeletion syndrome without cystinuria Occurrence Congenital true Inferred relationship Existential restriction modifier 2
2p21 microdeletion syndrome without cystinuria Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
2p21 microdeletion syndrome without cystinuria Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
2p21 microdeletion syndrome without cystinuria Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
2p21 microdeletion syndrome without cystinuria Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
2p21 microdeletion syndrome without cystinuria Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 2
2p21 microdeletion syndrome without cystinuria Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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