FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.12 | FHIR Version n/a User: [n/a]

399959003: Premature aging syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature aging syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Premature aging syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Premature aging syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome
\Disease\Congenital disease\Inborn error of metabolism\Premature aging syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

1767879012 Premature aging syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1773477015 Premature ageing syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

1774763010 Premature aging syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Premature aging syndrome	Is a	Hereditary disorder of the integument	true	Inferred relationship	Existential restriction modifier
Premature aging syndrome	Is a	Congenital anomaly of integument	false	Inferred relationship	Existential restriction modifier
Premature aging syndrome	Is a	Disorder of skin	true	Inferred relationship	Existential restriction modifier
Premature aging syndrome	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier
Premature aging syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Premature aging syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hutchinson-Gilford syndrome	Is a	False	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Metageria	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Acrogeria	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Neonatal pseudo-hydrocephalic progeroid syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Wrinkly skin syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Geroderma osteodysplastica	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Werner syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Progeroid short stature with pigmented nevi	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Atypical Werner syndrome	Is a	False	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Ehlers-Danlos syndrome progeroid type	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Pseudoprogeria syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Progeroid syndrome Petty type	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Ogden syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Nestor Guillermo progeria syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Lamin A/C related cardiocutaneous progeria syndrome	Is a	False	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Progeroid and marfanoid aspect, lipodystrophy syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Acroosteolysis, keloid-like lesions, premature aging syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Leprechaunism syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Laminopathy with premature aging	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Progeroid features, hepatocellular carcinoma predisposition syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier
Keppen Lubinsky syndrome	Is a	True	Premature aging syndrome	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1767879012	Premature aging syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1773477015	Premature ageing syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1774763010	Premature aging syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module