773426004: Lamin A/C related cardiocutaneous progeria syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Cardiovascular finding\Disorder of cardiovascular system\Cardiovascular system hereditary disorder\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Disorder of body system\Disorder of cardiovascular system\Cardiovascular system hereditary disorder\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Congenital disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Lamin A/C related cardiocutaneous progeria syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3723511014	Lamin A/C related cardiocutaneous progeria syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3723512019	LMNA-related cardiocutaneous progeria syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3723513012	Lamin A/C related cardiocutaneous progeria syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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