FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

699669001: Renpenning syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2985438013 Renpenning syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2985573013 Renpenning syndrome en Synonym Active Case insensitive SNOMED CT core
2985599018 Porteous syndrome en Synonym Active Case insensitive SNOMED CT core
2985812018 Sutherland-Haan syndrome en Synonym Active Case sensitive SNOMED CT core
2985846017 X-linked intellectual deficit due to PQBP1 mutation en Synonym Active Initial character case insensitive SNOMED CT core
2985874010 Hamel cerebropalatocardiac syndrome en Synonym Active Case insensitive SNOMED CT core
2987369010 Golabi-Ito-Hall syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Renpenning syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Renpenning syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Renpenning syndrome Is a X-linked recessive hereditary disease true Inferred relationship Some
Renpenning syndrome Interprets Intellectual ability true Inferred relationship Some 2
Renpenning syndrome Has interpretation Impaired true Inferred relationship Some 2
Renpenning syndrome Interprets Adaptation behaviour true Inferred relationship Some 3
Renpenning syndrome Has interpretation Impaired true Inferred relationship Some 3
Renpenning syndrome Is a X-linked hereditary disease false Inferred relationship Some
Renpenning syndrome Is a Intellectual disability false Inferred relationship Some
Renpenning syndrome Is a Intellectual disability true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start