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715630006: melanosis diffusa congenita (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3303231011 Familial progressive hyperpigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303232016 Melanosis diffusa congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303233014 Melanosis universalis hereditaria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303234015 Universal melanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6195671000146118 melanosis diffusa congenita (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6195681000146116 melanosis diffusa congenita nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6195701000146119 melanosis universalis hereditaria nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6719961000146110 familiaire progressieve hyperpigmentatie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial progressive hyperpigmentation (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial progressive hyperpigmentation (disorder) Is a Hereditary disorder of the integument false Inferred relationship Some
Familial progressive hyperpigmentation (disorder) Is a Hereditary hypermelanosis (disorder) true Inferred relationship Some
Familial progressive hyperpigmentation (disorder) Associated morphology Melanosis true Inferred relationship Some 1
Familial progressive hyperpigmentation (disorder) Finding site Skin structure true Inferred relationship Some 1
Familial progressive hyperpigmentation (disorder) Is a Genetic disorder of skin pigmentation (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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