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765195000: Familial generalized lentiginosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3657404011 Familial generalised lentiginosis en Synonym Active Entire term case insensitive SNOMED CT core module
3657405012 Familial generalized lentiginosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3657406013 Familial generalized lentiginosis en Synonym Active Entire term case insensitive SNOMED CT core module
3657407016 Familial multiple lentigines syndrome without systemic involvement en Synonym Active Entire term case insensitive SNOMED CT core module
3657408014 Familial lentigines profusa 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
Familial generalized lentiginosis Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Familial generalized lentiginosis Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial generalized lentiginosis Is a Lentiginosis true Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Is a Genetic disorder of skin pigmentation false Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Associated morphology Lentigo true Inferred relationship Existential restriction modifier 1
Familial generalized lentiginosis Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Is a Congenital hamartoma of skin true Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Is a Congenital melanosis true Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Familial generalized lentiginosis Is a Hereditary hypermelanosis true Inferred relationship Existential restriction modifier
Familial generalized lentiginosis Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Arterial dissection and lentiginosis syndrome Is a False Familial generalized lentiginosis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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