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715630006: Familial progressive hyperpigmentation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3303230012 Familial progressive hyperpigmentation (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303231011 Familial progressive hyperpigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
3303232016 Melanosis diffusa congenita en Synonym Active Entire term case insensitive SNOMED CT core module
3303233014 Melanosis universalis hereditaria en Synonym Active Entire term case insensitive SNOMED CT core module
3303234015 Universal melanosis 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 progressive hyperpigmentation Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation Is a Hereditary hypermelanosis true Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation Associated morphology Melanosis true Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation Is a Genetic disorder of skin pigmentation false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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