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11528001: Mucinosis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
19928014 Mucinosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
666867014 Mucinosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mucinosis Is a Deposition true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Focal oral mucinosis (finding) Associated morphology False Mucinosis Inferred relationship Some 1
Focal cutaneous mucinosis Associated morphology False Mucinosis Inferred relationship Some 1
Acral persistent papular mucinosis (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Lichen myxedematosus Associated morphology False Mucinosis Inferred relationship Some 2
Alopecia mucinosa Associated morphology False Mucinosis Inferred relationship Some 2
Scleromyxedema (disorder) Associated morphology False Mucinosis Inferred relationship Some 2
Diffuse cutaneous mucinosis (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Reticular erythematous mucinosis Associated morphology False Mucinosis Inferred relationship Some 1
Self-healing juvenile cutaneous mucinosis Associated morphology False Mucinosis Inferred relationship Some 1
Idiopathic benign cutaneous mucinosis Associated morphology False Mucinosis Inferred relationship Some 1
Mucinosis affecting skin (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Focal primary mucinosis of skin (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Secondary catabolic mucinosis of skin (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Lupus erythematosus-associated papulonodular mucinosis (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Follicular mucinosis type mycosis fungoides (disorder) Associated morphology True Mucinosis Inferred relationship Some 2
Idiopathic benign cutaneous mucinosis Associated morphology False Mucinosis Inferred relationship Some 1
Alopecia mucinosa Associated morphology True Mucinosis Inferred relationship Some 2
Reticular erythematous mucinosis Associated morphology True Mucinosis Inferred relationship Some 1
Focal cutaneous mucinosis Associated morphology True Mucinosis Inferred relationship Some 1
Focal oral mucinosis (finding) Associated morphology True Mucinosis Inferred relationship Some 1
Lupus erythematosus-associated papulonodular mucinosis (disorder) Associated morphology True Mucinosis Inferred relationship Some 1
Secondary catabolic mucinosis of skin (disorder) Associated morphology True Mucinosis Inferred relationship Some 1
Mucinosis affecting skin (disorder) Associated morphology True Mucinosis Inferred relationship Some 1
Focal primary mucinosis of skin (disorder) Associated morphology True Mucinosis Inferred relationship Some 1
Acral persistent papular mucinosis (disorder) Associated morphology False Mucinosis Inferred relationship Some 1
Diffuse cutaneous mucinosis (disorder) Associated morphology True Mucinosis Inferred relationship Some 1
Self-healing juvenile cutaneous mucinosis Associated morphology False Mucinosis Inferred relationship Some 1
Nodular lichen myxedematosus is a rare form of localized lichen myxedematosus characterized by the development of skin-coloured mucinous nodules on the limbs and trunk, with mild or absent papular eruption. Associated morphology False Mucinosis Inferred relationship Some 2
Discrete papular lichen myxedematosus is a rare chronic, slowly progressive form of localized lichen myxedematosus characterized by the development of a few to multiple small symmetrical skin-colored mucinous papules on the limbs and trunk. Associated morphology False Mucinosis Inferred relationship Some 2
Papular mucinosis of infancy is a rare pediatric non progressive form of localized lichen myxedematosus characterized by the development of firm opalescent mucinous papules on the upper arms and the trunk. Associated morphology False Mucinosis Inferred relationship Some 4
An intermediate form of lichen myxedematosus (LM) (a form of mucin dermal deposit) which does not meet the criteria for either scleromyxedema or the localized form. Three clinical subtypes have been described and include scleromyxedema without monoclonal gammopathy; localized forms with monoclonal gammopathy and/or systemic symptoms; localized forms with mixed features of the 5 subtypes of localized LM (discrete form, acral persistent papular mucinosis, self-healing papular mucinosis, papular mucinosis of infancy, and a pure nodular form). The course of atypical LM is unpredictable because only a few cases have been reported. Associated morphology False Mucinosis Inferred relationship Some 5
Pretibial myxedema Associated morphology True Mucinosis Inferred relationship Some 2
Graves' disease with pretibial myxedema AND with thyrotoxic crisis Associated morphology True Mucinosis Inferred relationship Some 4
Circumscribed nodular and tuberous pretibial myxedema (disorder) Associated morphology True Mucinosis Inferred relationship Some 3
Diffuse pretibial myxedema (disorder) Associated morphology True Mucinosis Inferred relationship Some 3
Elephantiasic pretibial myxedema (disorder) Associated morphology True Mucinosis Inferred relationship Some 3
Toxic diffuse goiter with pretibial myxedema Associated morphology True Mucinosis Inferred relationship Some 7
Lichen mucinosis Is a True Mucinosis Inferred relationship Some

This concept is not in any reference sets

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