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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


16 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital melanosis Is a Congenital anomaly of integument false Inferred relationship Some
Congenital melanosis Associated morphology Congenital hyperpigmentation false Inferred relationship Some 2
Congenital melanosis Occurrence Congenital true Inferred relationship Some 1
Congenital melanosis Finding site Skin structure false Inferred relationship Some 1
Congenital melanosis Associated morphology Melanosis true Inferred relationship Some 1
Congenital melanosis Is a Congenital anomaly of skin false Inferred relationship Some
Congenital melanosis Is a Skin lesion false Inferred relationship Some
Congenital melanosis Finding site Skin structure false Inferred relationship Some 4
Congenital melanosis Finding site Skin structure false Inferred relationship Some 4
Congenital melanosis Finding site Skin structure false Inferred relationship Some 2
Congenital melanosis Finding site Skin structure false Inferred relationship Some 2
Congenital melanosis Finding site Skin structure false Inferred relationship Some 1
Congenital melanosis Is a Melanosis (disorder) true Inferred relationship Some
Congenital melanosis Is a Congenital malformation false Inferred relationship Some
Congenital melanosis Occurrence Congenital false Inferred relationship Some 2
Congenital melanosis Is a Congenital disease (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital melanosis of sclera Is a True Congenital melanosis Inferred relationship Some
Hypotrichosis with keratosis pilaris and lentiginosis Is a False Congenital melanosis Inferred relationship Some
Centrofacial lentiginosis syndrome Is a True Congenital melanosis Inferred relationship Some
Hereditary benign acanthosis nigricans with insulin resistance Is a True Congenital melanosis Inferred relationship Some
Peutz-Jeghers syndrome Is a True Congenital melanosis Inferred relationship Some
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome Is a True Congenital melanosis Inferred relationship Some
Familial generalised lentiginosis Is a True Congenital melanosis Inferred relationship Some
Hereditary benign acanthosis nigricans Is a True Congenital melanosis Inferred relationship Some
Acromelanosis Is a True Congenital melanosis Inferred relationship Some
Neurocutaneous melanosis sequence Is a False Congenital melanosis Inferred relationship Some
Melanosis oculi (disorder) Is a True Congenital melanosis Inferred relationship Some
Arterial dissection and lentiginosis syndrome (disorder) Is a True Congenital melanosis Inferred relationship Some
Nevus spilus (disorder) Is a True Congenital melanosis Inferred relationship Some
Neurocutaneous melanosis Is a True Congenital melanosis Inferred relationship Some

Reference Sets

GB English

US English

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