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703541007: Neurofibromatosis type 1-like syndrome (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neurofibromatosis type 1-like syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Neurofibromatosis type 1-like syndrome Is a Café au lait spot true Inferred relationship Existential restriction modifier
Neurofibromatosis type 1-like syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Neurofibromatosis type 1-like syndrome Associated morphology Pigment alteration false Inferred relationship Existential restriction modifier 1
Neurofibromatosis type 1-like syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Neurofibromatosis type 1-like syndrome Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Neurofibromatosis type 1-like syndrome Is a Hyperpigmentation of skin true Inferred relationship Existential restriction modifier
Neurofibromatosis type 1-like syndrome Is a Congenital disease true Inferred relationship Existential restriction modifier
Neurofibromatosis type 1-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Neurofibromatosis type 1-like syndrome Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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