773644000: Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Finding of head and neck region\Head finding\...
• \Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Genetic disease\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Genetic disease\Hereditary disease\Inherited disorder of connective tissue\Marfan's syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Marfan's syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Degenerative disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of connective tissue\Inherited disorder of connective tissue\Marfan's syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of connective tissue\Congenital connective tissue disorder\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of connective tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Congenital disease\Congenital connective tissue disorder\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Congenital disease\Inborn error of metabolism\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Progeroid and marfanoid aspect, lipodystrophy syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of subcutaneous tissue\Progeroid and marfanoid aspect, lipodystrophy syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3725348019	Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3725349010	Progeroid and marfanoid aspect, lipodystrophy syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3725350010	A rare systemic disease characterised by a neonatal progeroid appearance (not associated with other manifestations of premature ageing) associated with facial dysmorphism (for example macrocephaly or arrested hydrocephaly, proptosis, downslanting palpebral fissures, retrognathia), generalised extreme congenital lack of subcutaneous fat tissue (except in the breast and iliac region) and incomplete signs of Marfan syndrome (mainly severe myopia, joint hyperextensibility and arachnodactyly). Metabolic disturbances are not associated. There is evidence the disease is caused by heterozygous mutation in the FBN1 gene on chromosome 15q21.	en	Definition	Active	Case sensitive	SNOMED CT core
3725351014	A rare systemic disease characterized by a neonatal progeroid appearance (not associated with other manifestations of premature aging) associated with facial dysmorphism (for example macrocephaly or arrested hydrocephaly, proptosis, downslanting palpebral fissures, retrognathia), generalized extreme congenital lack of subcutaneous fat tissue (except in the breast and iliac region) and incomplete signs of Marfan syndrome (mainly severe myopia, joint hyperextensibility and arachnodactyly). Metabolic disturbances are not associated. There is evidence the disease is caused by heterozygous mutation in the FBN1 gene on chromosome 15q21.	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

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