238874008: Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome

\Finding of neonate\Neonatal disorder\Neonatal metabolic disorder (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Fetal and/or neonatal disorder\Congenital disease\Inborn error of metabolism\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Fetal and/or neonatal disorder\Neonatal disorder\Neonatal metabolic disorder (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Metabolic disease\Neonatal metabolic disorder (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	Progeria	false	Inferred relationship	Some
Neonatal pseudo-hydrocephalic progeroid syndrome	Finding site	Skin structure	true	Inferred relationship	Some	2
Neonatal pseudo-hydrocephalic progeroid syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	Premature aging syndrome (disorder)	true	Inferred relationship	Some
Neonatal pseudo-hydrocephalic progeroid syndrome	Occurrence	Neonatal	true	Inferred relationship	Some	3
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	Neonatal disorder	false	Inferred relationship	Some
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	Neonatal metabolic disorder (disorder)	true	Inferred relationship	Some
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	Fetal and/or neonatal disorder of integument	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
358004015	Neonatal pseudo-hydrocephalic progeroid syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
358005019	Wiedemann-Rautenstrauch syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
627813012	Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
7264411000241112	syndrome progéroïde néonatal	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
7264421000241117	syndrome de Wiedemann-Rautenstrauch	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
7264431000241115	syndrome progéroïde pseudo-hydrocéphalique néonatal	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3453501001000117	Wiedemann-Rautenstrauch-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module