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1260467009: Large congenital pigmented melanocytic nevus of skin (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5400449012 A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400450012 A rare skin hamartoma characterised by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic naevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganised epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160592011 GCMN - giant congenital melanocytic naevus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160593018 LCMN - large congenital melanocytic naevus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160594012 LCMN - large congenital melanocytic nevus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160596014 Giant congenital melanocytic naevus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160597017 Large congenital pigmented melanocytic nevus of skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160598010 GCMN - giant congenital melanocytic nevus en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5160600016 Giant congenital melanocytic nevus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160603019 Large congenital pigmented melanocytic nevus of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5160604013 Large congenital pigmented melanocytic naevus of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Is a Congenital pigmented melanocytic nevus of skin (disorder) true Inferred relationship Some
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Is a Genetic disease true Inferred relationship Some
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Occurrence Congenital true Inferred relationship Some 1
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Finding site Skin structure true Inferred relationship Some 1
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Associated morphology Pigmented nevus false Inferred relationship Some 1
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Associated morphology Congenital melanocytic nevus (morphologic abnormality) true Inferred relationship Some 1
A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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