1003923009: Rothmund Thomson syndrome type 2 (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\Rothmund Thomson syndrome type 2
• \Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \General finding of soft tissue\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \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\Rothmund Thomson syndrome type 2
• \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\Rothmund Thomson syndrome type 2
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \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\Rothmund Thomson syndrome type 2
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Integumentary system finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Hereditary neoplastic syndrome\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Rothmund Thomson syndrome type 2
• \Disease\Degenerative disorder\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \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\Rothmund Thomson syndrome type 2
• \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\Rothmund Thomson syndrome type 2
• \Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \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\Rothmund Thomson syndrome type 2
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Developmental disorder\Developmental hereditary disorder\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Rothmund-Thomson syndrome\Rothmund Thomson syndrome type 2

Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4166978011	Rothmund Thomson syndrome type 2	en	Synonym	Active	Case sensitive	SNOMED CT core
4166979015	Rothmund Thomson syndrome type 2 (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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