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399959003: Premature aging syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
1767879012 Premature aging syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773477015 Premature ageing syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774763010 Premature aging syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1767879012 Premature aging syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1767879012 Premature aging syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773477015 Premature ageing syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1773477015 Premature ageing syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774763010 Premature aging syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1774763010 Premature aging syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3422551001000111 Alterung, vorzeitige de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5257821000241117 syndrome de sénilité précoce fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5257821000241117 syndrome de sénilité précoce fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3422551001000111 Alterung, vorzeitige de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

24 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Premature aging syndrome (disorder) Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Premature aging syndrome (disorder) Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier (core metadata concept)
Premature aging syndrome (disorder) Is a Disorder of skin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Premature aging syndrome (disorder) Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Premature aging syndrome (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Premature aging syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hutchinson-Gilford syndrome Is a False Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Metageria Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Acrogeria Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal pseudo-hydrocephalic progeroid syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Wrinkly skin syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Geroderma osteodysplastica Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Werner syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progeroid short stature with pigmented nevi (disorder) Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Atypical Werner syndrome (disorder) Is a False Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ehlers-Danlos syndrome progeroid type Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Pseudoprogeria syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progeroid syndrome Petty type Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ogden syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Nestor Guillermo progeria syndrome (disorder) Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Mandibular hypoplasia, deafness, progeroid syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
LMNA-related cardiocutaneous progeria syndrome Is a False Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder) Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Acroosteolysis, keloid-like lesions, premature ageing syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Leprechaunism syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Laminopathy with premature aging (disorder) Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare inherited cancer-predisposing syndrome characterised by early-onset hepatocellular carcinoma, genomic instability, and progeroid features, such as short stature, low body weight, muscular atrophy, lipodystrophy, bilateral cataracts, and premature hair greying. Dysmorphic craniofacial features include triangular face, small, deep-set eyes, and micrognathia. Kyphoscoliosis, sloping shoulders, mild pectus excavatum, bilateral contractures of the elbows and fingers, bilateral clinodactyly, and pes planus have also been reported. Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Keppen Lubinsky syndrome Is a True Premature aging syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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