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703541007: Neurofibromatosis type 1-like syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3008946013 Legius syndrome en Synonym Active Case sensitive SNOMED CT core
3009354011 Neurofibromatosis type 1-like syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3009678012 NFLS - neurofibromatosis type 1-like syndrome en Synonym Active Case sensitive SNOMED CT core
3009772019 Neurofibromatosis type 1-like syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Legius syndrome Is a Hyperpigmentation of skin true Inferred relationship Some
Legius syndrome Is a Congenital disease true Inferred relationship Some
Legius syndrome Occurrence Congenital true Inferred relationship Some 1
Legius syndrome Associated morphology Hyperpigmentation true Inferred relationship Some 1
Legius syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Legius syndrome Is a Café au lait spots true Inferred relationship Some
Legius syndrome Is a Hereditary disorder of the integument true Inferred relationship Some
Legius syndrome Associated morphology Pigment alteration false Inferred relationship Some 1
Legius syndrome Finding site Skin structure true Inferred relationship Some 1
Legius syndrome Is a Genetic disorder of skin pigmentation 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

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