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776417008: Acroosteolysis, keloid-like lesions, premature aging syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3736343010 Acroosteolysis, keloid-like lesions, premature ageing syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3736344016 Acroosteolysis, keloid-like lesions, premature aging syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3736345015 Premature aging syndrome, Penttinen type en Synonym Active Only initial character case insensitive SNOMED CT core module
3736346019 Acroosteolysis, keloid-like lesions, premature aging syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3736347011 Premature ageing syndrome Penttinen type en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acroosteolysis, keloid-like lesions, premature aging syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Acroosteolysis, keloid-like lesions, premature aging syndrome Is a Premature aging syndrome true Inferred relationship Existential restriction modifier
Acroosteolysis, keloid-like lesions, premature aging syndrome Is a Acroosteolysis false Inferred relationship Existential restriction modifier
Acroosteolysis, keloid-like lesions, premature aging syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Acroosteolysis, keloid-like lesions, premature aging syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Acroosteolysis, keloid-like lesions, premature aging syndrome Is a Metabolic bone disease true Inferred relationship Existential restriction modifier
Acroosteolysis, keloid-like lesions, premature aging syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Acroosteolysis, keloid-like lesions, premature aging syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Acroosteolysis, keloid-like lesions, premature aging syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Acroosteolysis, keloid-like lesions, premature aging syndrome Is a Hereditary acroosteolysis true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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