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715630006: Familial progressive hyperpigmentation (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303230012 Familial progressive hyperpigmentation (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3303231011 Familial progressive hyperpigmentation en Synonym Active Case insensitive SNOMED CT core
3303232016 Melanosis diffusa congenita en Synonym Active Case insensitive SNOMED CT core
3303233014 Melanosis universalis hereditaria en Synonym Active Case insensitive SNOMED CT core
3303234015 Universal melanosis en Synonym Active Case insensitive SNOMED CT core
3303235019 Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder. en Definition Active Case sensitive SNOMED CT core


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 Some
Familial progressive hyperpigmentation Is a Hereditary disorder of the integument false Inferred relationship Some
Familial progressive hyperpigmentation Is a Hereditary hypermelanosis true Inferred relationship Some
Familial progressive hyperpigmentation Associated morphology Melanosis true Inferred relationship Some 1
Familial progressive hyperpigmentation Finding site Skin structure true Inferred relationship Some 1
Familial progressive hyperpigmentation Is a Genetic disorder of skin pigmentation false 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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