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239079007: Inherited cutaneous hyperpigmentation (disorder)


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
358290010 Inherited cutaneous hyperpigmentation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
6312221000241119 hyperpigmentation héréditaire de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6312231000241117 hyperpigmentation cutanée héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6312221000241119 hyperpigmentation héréditaire de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6312231000241117 hyperpigmentation cutanée héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Is a Hyperpigmentation of skin true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited cutaneous hyperpigmentation Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited cutaneous hyperpigmentation Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited cutaneous hyperpigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Inherited cutaneous hyperpigmentation Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Inherited cutaneous hyperpigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Inherited cutaneous hyperpigmentation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Associated morphology Hyperpigmentation (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited cutaneous hyperpigmentation Is a Genetic disorder of skin pigmentation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited cutaneous hyperpigmentation Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

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

This concept is not in any reference sets

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