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773702002: Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3725847019 Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725848012 Interleukin-1 receptor antagonist deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725849016 OMPP - sterile osteomyelitis, multifocal with periostitis and pustulosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3725850016 Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725851017 Sterile multifocal osteomyelitis with periostitis and pustulosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725852012 A rare severe genetic autoinflammatory syndrome characterised by usually neonatal onset of generalised neutrophilic cutaneous pustulosis and severe recurrent multifocal aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features. Caused by homozygous mutation in the IL1RN gene on chromosome 2q14. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3725853019 A rare severe genetic autoinflammatory syndrome characterized by usually neonatal onset of generalized neutrophilic cutaneous pustulosis and severe recurrent multifocal aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features. Caused by homozygous mutation in the IL1RN gene on chromosome 2q14. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3725847019 Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725848012 Interleukin-1 receptor antagonist deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725849016 OMPP - sterile osteomyelitis, multifocal with periostitis and pustulosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3725850016 Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725851017 Sterile multifocal osteomyelitis with periostitis and pustulosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3725852012 A rare severe genetic autoinflammatory syndrome characterised by usually neonatal onset of generalised neutrophilic cutaneous pustulosis and severe recurrent multifocal aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features. Caused by homozygous mutation in the IL1RN gene on chromosome 2q14. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3725853019 A rare severe genetic autoinflammatory syndrome characterized by usually neonatal onset of generalized neutrophilic cutaneous pustulosis and severe recurrent multifocal aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features. Caused by homozygous mutation in the IL1RN gene on chromosome 2q14. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3428571001000119 Sterile multifokale Osteomyelitis mit Periostitis und Pustulose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887471000172113 ostéomyélite stérile multifocale avec périostéite et pustulose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1015961000172115 DIRA - disease due to interleukin-1 receptor antagonist deficiency fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887471000172113 ostéomyélite stérile multifocale avec périostéite et pustulose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1015961000172115 DIRA - disease due to interleukin-1 receptor antagonist deficiency fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428571001000119 Sterile multifokale Osteomyelitis mit Periostitis und Pustulose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Associated morphology Pustule true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Inflammatory disorder of immune system false Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Hereditary disorder of immune system true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Primary immune deficiency disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Skeletal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Neonatal dermatosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Skin lesion false Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Vesicle of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Pustule (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Occurrence Fetal or neonatal period false Inferred relationship Existential restriction modifier (core metadata concept) 5
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Disorder involving the integument of fetus OR newborn false Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Is a Autoinflammatory disease true Inferred relationship Existential restriction modifier (core metadata concept)
Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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