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86042009: Congenital melanosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
142649017 Congenital melanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
828223014 Congenital melanosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital melanosis (disorder) est un(e) (attribut) Congenital anomaly of skin false Inferred relationship Some
Congenital melanosis (disorder) est un(e) (attribut) Skin lesion false Inferred relationship Some
Congenital melanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
Congenital melanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
Congenital melanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital melanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Congenital melanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital melanosis (disorder) est un(e) (attribut) Melanosis (disorder) true Inferred relationship Some
Congenital melanosis (disorder) est un(e) (attribut) Congenital anomaly of integument false Inferred relationship Some
Congenital melanosis (disorder) est un(e) (attribut) Congenital malformation false Inferred relationship Some
Congenital melanosis (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Congenital melanosis (disorder) morphologie associée (attribut) Congenital hyperpigmentation (morphologic abnormality) false Inferred relationship Some 2
Congenital melanosis (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital melanosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Congenital melanosis (disorder) morphologie associée (attribut) mélanose (anomalie morphologique) true Inferred relationship Some 1
Congenital melanosis (disorder) est un(e) (attribut) Congenital disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Acromelanosis est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Neurocutaneous melanosis sequence est un(e) (attribut) False Congenital melanosis (disorder) Inferred relationship Some
mélanose oculaire est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Arterial dissection and lentiginosis syndrome (disorder) est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Nevus spilus (disorder) est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Neurocutaneous melanosis est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Congenital melanosis of sclera (disorder) est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Hypotrichosis with keratosis pilaris and lentiginosis est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Centrofacial lentiginosis syndrome est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
acanthosis nigricans héréditaire bénin avec insulinorésistance est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
lentiginose périorificielle avec polypose viscérale est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Familial generalised lentiginosis est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some
Hereditary benign acanthosis nigricans est un(e) (attribut) True Congenital melanosis (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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