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699669001: Renpenning syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2985438013 Renpenning syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2985573013 Renpenning syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2985599018 Porteous syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2985812018 Sutherland-Haan syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2985846017 X-linked intellectual deficit due to PQBP1 mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
2985874010 Hamel cerebropalatocardiac syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2987369010 Golabi-Ito-Hall 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
Renpenning syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Renpenning syndrome Is a Mental retardation false Inferred relationship Existential restriction modifier
Renpenning syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
Renpenning syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Renpenning syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Renpenning syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier
Renpenning syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 2
Renpenning syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 2
Renpenning syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 3
Renpenning syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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