890434000: Cockayne syndrome type 2 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Hereditary neoplastic syndrome\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Disorder of body system\Neurological disorder\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Congenital anomaly of central nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Developmental disorder\Developmental hereditary disorder\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with senile-like appearance\Cockayne syndrome\Cockayne syndrome type 2
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Cockayne syndrome\Cockayne syndrome type 2

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4012561012	Cockayne syndrome type 2	en	Synonym	Active	Case sensitive	SNOMED CT core
4012562017	Cockayne syndrome type 2 (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
4016113014	Early onset Cockayne syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4016114015	Cockayne syndrome is a rare autosomal recessive disease, manifestations may include short stature, progeria, photosensitivity, and learning delay, failure to thrive in the newborn, microcephaly, neurological developmental delay. Type 2 Cockayne syndrome, also known as 'severe' or 'early onset' usually presents in at or soon after birth.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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