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239091003: Dermatosis of infancy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
358308010 Dermatosis of infancy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
628060017 Dermatosis of infancy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5852941000241114 maladie de la peau durant la petite enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5852951000241112 affection cutanée dans la petite enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5852961000241110 dermatose au cours de la petite enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

79 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dermatosis of infancy Is a Age, sex or race-related dermatoses false Inferred relationship Some
Dermatosis of infancy Finding site Skin structure false Inferred relationship Some 3
Dermatosis of infancy Is a Disorder of skin (disorder) false Inferred relationship Some
Dermatosis of infancy Occurrence Infancy true Inferred relationship Some 1
Dermatosis of infancy Is a atteintes affectant les téguments et/ou la régulation de la température du fœtus ou du nouveau-né false Inferred relationship Some
Dermatosis of infancy Occurrence Fetal or neonatal period false Inferred relationship Some 2
Dermatosis of infancy Is a Disorder of skin and/or subcutaneous tissue (disorder) true Inferred relationship Some
Dermatosis of infancy Finding site Skin and/or subcutaneous tissue structure (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Lamellar ichthyosis Is a False Dermatosis of infancy Inferred relationship Some
Omphalitis (disorder) Is a False Dermatosis of infancy Inferred relationship Some
Acropustulosis of infancy Is a True Dermatosis of infancy Inferred relationship Some
Fetal and/or neonatal disorder of integument Is a False Dermatosis of infancy Inferred relationship Some
érythème toxique Is a False Dermatosis of infancy Inferred relationship Some
Sclerema Is a False Dermatosis of infancy Inferred relationship Some
Omphalitis of newborn (disorder) Is a False Dermatosis of infancy Inferred relationship Some
Infantile erythroderma, failure to thrive and diarrhea syndrome (disorder) Is a True Dermatosis of infancy Inferred relationship Some
dermatite séborrhéique infantile Is a False Dermatosis of infancy Inferred relationship Some
Sclerema neonatorum Is a True Dermatosis of infancy Inferred relationship Some
Urticaria neonatorum Is a False Dermatosis of infancy Inferred relationship Some
Fibrous hamartoma of infancy Is a True Dermatosis of infancy Inferred relationship Some
Infantile atopic dermatitis (disorder) Is a False Dermatosis of infancy Inferred relationship Some
Neonatal dermatosis (disorder) Is a True Dermatosis of infancy Inferred relationship Some
Generalized seborrheic dermatitis of infants Is a True Dermatosis of infancy Inferred relationship Some
Michelin-tyre baby Is a True Dermatosis of infancy Inferred relationship Some
Subcutaneous fat necrosis of newborn Is a True Dermatosis of infancy Inferred relationship Some
Infantile stiff skin syndrome (disorder) Is a True Dermatosis of infancy Inferred relationship Some
Cutaneous mastocytosis, infantile form (disorder) Is a True Dermatosis of infancy Inferred relationship Some
Infantile eczema Is a True Dermatosis of infancy Inferred relationship Some
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Is a True Dermatosis of infancy Inferred relationship Some
Infantile acne Is a True Dermatosis of infancy Inferred relationship Some
Cradle cap Is a True Dermatosis of infancy Inferred relationship Some
Miliaria crystallina, infantile (disorder) Is a True Dermatosis of infancy Inferred relationship Some
Erythroderma in infancy Is a True Dermatosis of infancy Inferred relationship Some
Panniculitis in newborn Is a True Dermatosis of infancy Inferred relationship Some
Infantile pustular psoriasis Is a True Dermatosis of infancy Inferred relationship Some
Warts of perianal region in infancy caused by human papillomavirus (disorder) Is a True Dermatosis of infancy Inferred relationship Some
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands. Is a False Dermatosis of infancy Inferred relationship Some
Infantile digital fibromatosis (disorder) Is a True Dermatosis of infancy Inferred relationship Some
Miliaria rubra, infantile (disorder) Is a True Dermatosis of infancy Inferred relationship Some
A rare genetic systemic or rheumatologic disease characterized by infantile onset of skin anomalies (such as delayed wound healing with atrophic scars and mild alopecia with dry and brittle hair), retinal rod degeneration with night blindness, degenerative myopathy with muscle weakness, myalgia, and cramps, osteoarthritis, joint laxity, prolapse of internal organs, floating kidney syndrome, malabsorption syndrome, and hypothyroidism. The phenotype has been reported to be more severe in women than in men. Is a True Dermatosis of infancy Inferred relationship Some
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. Is a True Dermatosis of infancy Inferred relationship Some
Infantile pedal papules Is a True Dermatosis of infancy Inferred relationship Some

This concept is not in any reference sets

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