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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


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inherited cutaneous hyperpigmentation Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation morphologie associée (attribut) Hyperpigmentation (morphologic abnormality) true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation est un(e) (attribut) Genetic disorder of skin pigmentation (disorder) true Inferred relationship Some
Inherited cutaneous hyperpigmentation est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Inherited cutaneous hyperpigmentation morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation est un(e) (attribut) Site-specific disorder of skin false Inferred relationship Some
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation survenue (attribut) congénital false Inferred relationship Some 3
Inherited cutaneous hyperpigmentation morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
Inherited cutaneous hyperpigmentation survenue (attribut) congénital false Inferred relationship Some
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some 1
Inherited cutaneous hyperpigmentation morphologie associée (attribut) Hyperpigmentation (morphologic abnormality) false Inferred relationship Some 2
Inherited cutaneous hyperpigmentation est un(e) (attribut) Genodermatosis true Inferred relationship Some
Inherited cutaneous hyperpigmentation est un(e) (attribut) hyperpigmentation de la peau true Inferred relationship Some
Inherited cutaneous hyperpigmentation survenue (attribut) congénital true Inferred relationship Some 1
Inherited cutaneous hyperpigmentation est un(e) (attribut) anomalies congénitales de pigmentation de la peau true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteopathia striata, pigmentary dermopathy, white forelock syndrome est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Hereditary benign acanthosis nigricans est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
acanthosis nigricans héréditaire bénin avec insulinorésistance est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Normal variation in cutaneous pigmentation (finding) est un(e) (attribut) False Inherited cutaneous hyperpigmentation Inferred relationship Some
Dyschromatosis universalis est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Naegeli-Franceschetti-Jadassohn syndrome est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Symmetrical dyschromatosis of extremities est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Zosteriform reticulate hyperpigmentation est un(e) (attribut) False Inherited cutaneous hyperpigmentation Inferred relationship Some
Dermatopathia pigmentosa reticularis est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
Acromelanosis est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) est un(e) (attribut) False Inherited cutaneous hyperpigmentation Inferred relationship Some
syndrome de dysplasie osseuse terminale-défauts de pigmentation est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
syndrome d'hypoplasie du pouce-alopécie-anomalie de la pigmentation est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some
syndrome d'extrasystoles, petite taille, hyperpigmentation, microcéphalie est un(e) (attribut) True Inherited cutaneous hyperpigmentation Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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