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239079007: hereditaire cutane hyperpigmentatie (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
358290010 Inherited cutaneous hyperpigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
628047011 Inherited cutaneous hyperpigmentation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
9908801000146111 erfelijke hyperpigmentatie van huid nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9908811000146113 hereditaire cutane hyperpigmentatie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9908821000146115 hereditaire cutane hyperpigmentatie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inherited cutaneous hyperpigmentation Is a Genodermatosis true Inferred relationship Some
Inherited cutaneous hyperpigmentation Is a Hyperpigmentation of skin true Inferred relationship Some
Inherited cutaneous hyperpigmentation Occurrence Congenital false Inferred relationship Some
Inherited cutaneous hyperpigmentation Finding site Skin structure true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Finding site Structure of skin region false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Associated morphology Hyperpigmentation false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation Is a Site-specific disorder of skin false Inferred relationship Some
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation Occurrence Congenital false Inferred relationship Some 3
Inherited cutaneous hyperpigmentation Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Some 3
Inherited cutaneous hyperpigmentation Occurrence Congenital true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Is a Congenital pigmentary skin anomalies true Inferred relationship Some
Inherited cutaneous hyperpigmentation Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Associated morphology Hyperpigmentation true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation Is a Genetic disorder of skin pigmentation (disorder) true Inferred relationship Some
Inherited cutaneous hyperpigmentation Is a Developmental hereditary disorder true Inferred relationship Some
Inherited cutaneous hyperpigmentation Is a Hereditary disorder of the integument true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Normal variation in cutaneous pigmentation Is a False Inherited cutaneous hyperpigmentation Inferred relationship Some
Dyschromatosis universalis Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Naegeli-Franceschetti-Jadassohn syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Symmetrical dyschromatosis of extremities Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Zosteriform reticulate hyperpigmentation Is a False Inherited cutaneous hyperpigmentation Inferred relationship Some
Dermatopathia pigmentosa reticularis Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Acromelanosis Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) Is a False Inherited cutaneous hyperpigmentation Inferred relationship Some
Terminal osseous dysplasia and pigmentary defect syndrome (disorder) Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Thumb deformity, alopecia, pigmentation anomaly syndrome (disorder) Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (disorder) Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Osteopathia striata, pigmentary dermopathy, white forelock syndrome Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Hereditary benign acanthosis nigricans Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Hereditary benign acanthosis nigricans with insulin resistance Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) Is a True Inherited cutaneous hyperpigmentation Inferred relationship Some

Reference Sets

GB English

US English

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