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\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Premature aging syndrome (disorder)\Neonatal pseudo-hydrocephalic progeroid syndrome
\Disease\Disorder of foetus and/or newborn\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:

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

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	Disorder involving the integument of fetus OR newborn	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

Back to Start

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