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254131007: Worth disease (disorder)

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
378302010 Autosomal dominant osteosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378303017 Worth disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644980017 Worth disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
378301015 Endosteal hyperostosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378302010 Autosomal dominant osteosclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378302010 Autosomal dominant osteosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378303017 Worth disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378303017 Worth disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644980017 Worth disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644980017 Worth disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3435371001000119 Endostale Hyperostose, Typ Worth de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5082061000241116 ostéosclérose autosomique dominante de type Worth fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5082061000241116 ostéosclérose autosomique dominante de type Worth fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3435371001000119 Endostale Hyperostose, Typ Worth 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
Worth disease Is a Endosteal hyperostoses (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Worth disease Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Worth disease Associated morphology Abnormally hard consistency false Inferred relationship Existential restriction modifier (core metadata concept)
Worth disease Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Worth disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Worth disease Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Worth disease Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Worth disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Worth disease Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 4
Worth disease Interprets Osteoclast turnover rate true Inferred relationship Existential restriction modifier (core metadata concept) 3
Worth disease Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Worth disease Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Worth disease Interprets Bone density scan true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Pulmonary histiocytosis X Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Eosinophilic granuloma of bone Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Langerhans cell histiocytosis, disseminated (disorder) Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Eosinophilic granuloma (disorder) Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary eosinophilic granuloma Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Hand-Schüller-Christian Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Langerhans cell histiocytosis Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Gastrointestinal eosinophilic granuloma Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Eosinophilic granuloma of oral mucosa Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Letterer-Siwe des ganglions lymphatiques intra-abdominaux Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Letterer-Siwe des ganglions lymphatiques intrapelviens Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Letterer-Siwe des ganglions intra thoraciques Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Letterer-Siwe disease of lymph nodes of axilla AND/OR upper limb Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Letterer-Siwe disease of lymph nodes of head, face AND/OR neck Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Letterer-Siwe disease of lymph nodes of inguinal region AND/OR lower limb Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Letterer-Siwe de ganglions lymphatiques de sites multiples Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Letterer-Siwe de la rate Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)
Letterer-Siwe disease of extranodal AND/OR solid organ site Course False Worth disease Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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