782910009: Seborrhea-like dermatitis with psoriasiform elements (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \General finding of soft tissue\Skin finding\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Seborrhoea-like dermatitis with psoriasiform elements
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Integumentary system finding\Skin finding\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammation of skin and/or subcutaneous tissue\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammation of skin and/or subcutaneous tissue\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Inflammatory dermatosis\Seborrhoea-like dermatitis with psoriasiform elements

Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3756654019	Seborrhea-like dermatitis with psoriasiform elements (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3756655018	Seborrhoea-like dermatitis with psoriasiform elements	en	Synonym	Active	Case insensitive	SNOMED CT core
3756656017	Seborrhea-like dermatitis with psoriasiform elements	en	Synonym	Active	Case insensitive	SNOMED CT core
3756657014	A rare genetic epidermal disorder with characteristics of a chronic diffuse fine scaly erythematous rash on the face (predominantly the chin, nasolabial folds, eyebrows) around the earlobes and over the scalp, associated with hyperkeratosis over elbows, knees, palms, soles and metacarpophalangeal joints, in the absence of associated rheumatological or neurological disorders. Cold weather, emotional stress and strenuous physical activity may exacerbate symptoms. There is evidence the disease is caused by mutation in the ZNF750 gene.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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