238874008: Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Finding of neonate\Neonatal disorder\Neonatal metabolic disorder\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Disorder of fetus or newborn\Neonatal disorder\Neonatal metabolic disorder\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Metabolic disease\Neonatal metabolic disorder\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Congenital disease\Inborn error of metabolism\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Neonatal pseudo-hydrocephalic progeroid syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
358004015	Neonatal pseudo-hydrocephalic progeroid syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
358005019	Wiedemann-Rautenstrauch syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
627813012	Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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