FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

403804008: Hereditary hypermelanosis (disorder)


Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771730019 Hereditary hypermelanosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
1782813016 Hereditary hypermelanosis en Synonym Active Case insensitive SNOMED CT core


13 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary hypermelanosis Is a Hereditary disorder of the integument true Inferred relationship Some
Hereditary hypermelanosis Is a Hyperpigmentation of skin true Inferred relationship Some
Hereditary hypermelanosis Finding site Structure of skin region false Inferred relationship Some 1
Hereditary hypermelanosis Associated morphology Hyperpigmentation false Inferred relationship Some 2
Hereditary hypermelanosis Is a Melanosis true Inferred relationship Some
Hereditary hypermelanosis Associated morphology Melanosis true Inferred relationship Some 1
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 1
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 2
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 1
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 2
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 1
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 2
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 1
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 2
Hereditary hypermelanosis Finding site Skin structure true Inferred relationship Some 1
Hereditary hypermelanosis Finding site Skin structure false Inferred relationship Some 2
Hereditary hypermelanosis Is a Genetic disorder of skin pigmentation true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Centrofacial lentiginosis syndrome Is a True Hereditary hypermelanosis Inferred relationship Some
Acromelanosis Is a True Hereditary hypermelanosis Inferred relationship Some
Familial generalised lentiginosis Is a True Hereditary hypermelanosis Inferred relationship Some
Arterial dissection and lentiginosis syndrome Is a True Hereditary hypermelanosis Inferred relationship Some
Hereditary benign acanthosis nigricans Is a True Hereditary hypermelanosis Inferred relationship Some
Hereditary benign acanthosis nigricans with insulin resistance Is a True Hereditary hypermelanosis Inferred relationship Some
Hypermelanotic pigmentary mosaicism Is a True Hereditary hypermelanosis Inferred relationship Some
Hereditary lentiginosis Is a False Hereditary hypermelanosis Inferred relationship Some
Hereditary diffuse melanosis Is a True Hereditary hypermelanosis Inferred relationship Some
Hereditary reticulate melanosis Is a True Hereditary hypermelanosis Inferred relationship Some
Genetic syndrome with hypermelanosis Is a True Hereditary hypermelanosis Inferred relationship Some
Familial progressive hyperpigmentation Is a True Hereditary hypermelanosis Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start