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724847001: Melanosis of mucosa of body orifice (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3444880015 Melanosis of mucosa of body orifice (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3444881016 Melanosis of mucosa of body orifice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3444882011 Mucosal melanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5946511000241110 mélanose de la muqueuse d'un orifice du corps fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Melanosis of mucosa of body orifice (disorder) Is a Disorder of mucous membrane (disorder) false Inferred relationship Some
Melanosis of mucosa of body orifice (disorder) Is a Lesion of mucosa true Inferred relationship Some
Melanosis of mucosa of body orifice (disorder) Is a Melanosis (disorder) true Inferred relationship Some
Melanosis of mucosa of body orifice (disorder) Is a Lesion of skin and/or skin-associated mucous membrane true Inferred relationship Some
Melanosis of mucosa of body orifice (disorder) Associated morphology Melanosis true Inferred relationship Some 1
Melanosis of mucosa of body orifice (disorder) Finding site Body orifice mucosa true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Characterized by irregular macular hyperpigmentation of the oral mucosa. Is a True Melanosis of mucosa of body orifice (disorder) Inferred relationship Some
Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome is a rare genetic ectodermal dysplasia syndrome characterized by short stature, nail dystrophy and/or nail loss, oral mucosa and/or tongue hyperpigmentation, dentition abnormalities (delayed teeth eruption, hypodontia, enamel hypoplasia), keratoderma on the margins of the palms and soles and focal hyperkeratosis on the dorsum of the hands and feet. Additionally, dysphagia with esophageal strictures, sensorineural deafness, bronchial asthma and severe iron-deficiency anemia have been observed. Is a True Melanosis of mucosa of body orifice (disorder) Inferred relationship Some
Buccal pigmentation due to Addison's disease (disorder) Is a True Melanosis of mucosa of body orifice (disorder) Inferred relationship Some
Melanotic macule of gingival mucosa Is a True Melanosis of mucosa of body orifice (disorder) Inferred relationship Some

This concept is not in any reference sets

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