69093006: Rothmund-Thomson syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...
• \Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Rothmund-Thomson syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary neoplastic syndrome\Rothmund-Thomson syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Rothmund-Thomson syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Rothmund-Thomson syndrome
• \Disease\Degenerative disorder\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Rothmund-Thomson syndrome
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Rothmund-Thomson syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Rothmund-Thomson syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Rothmund-Thomson syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Rothmund-Thomson syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
114761010	Rothmund-Thomson syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
114762015	Poikiloderma congenitale syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
1233118010	Poikiloderma congenitale	en	Synonym	Active	Case insensitive	SNOMED CT core
809000019	Rothmund-Thomson syndrome (disorder)	en	Fully specified name	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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