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702413000: RAPADILINO syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2995146017 RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence en Synonym Active Case sensitive SNOMED CT core
2995499018 RAPADILINO syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
2995600018 RAPADILINO syndrome en Synonym Active Case sensitive SNOMED CT core
3009673015 RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhoea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
RAPADILINO syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
RAPADILINO syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
RAPADILINO syndrome Is a Developmental hereditary disorder true Inferred relationship Some
RAPADILINO syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
RAPADILINO syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
RAPADILINO syndrome Occurrence Congenital true Inferred relationship Some 1
RAPADILINO syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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