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722287002: Autism and facial port-wine stain syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3331451017 Autism and facial port-wine stain syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3331452012 Autism and facial port-wine stain syndrome en Synonym Active Case insensitive SNOMED CT core
3331453019 Syndrome marked by the presence of a unilateral angioma on the face and autistic developmental problems with characteristics of language delay and atypical social interactions. So far, the syndrome has been described in four children. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autism and facial port-wine stain syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Autism and facial port-wine stain syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Autism and facial port-wine stain syndrome Is a Autistic disorder true Inferred relationship Some
Autism and facial port-wine stain syndrome Is a Port-wine stain of skin true Inferred relationship Some
Autism and facial port-wine stain syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Autism and facial port-wine stain syndrome Occurrence Congenital true Inferred relationship Some 1
Autism and facial port-wine stain syndrome Finding site Structure of capillary of skin true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Queensland allied health indicator for intervention reference set

Clinical finding foundation reference set

Mental health disorder reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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