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33979003: Nievergelt's syndrome (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
56730016 Nievergelt's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
56731017 Nievergelt-Erb syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
485700013 Mesomelic dysplasia - Nievergelt type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
765446011 Nievergelt's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2840192018 Nievergelt syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
56730016 Nievergelt's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
56731017 Nievergelt-Erb syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
485700013 Mesomelic dysplasia - Nievergelt type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
765446011 Nievergelt's syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
765446011 Nievergelt's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2840192018 Nievergelt syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3391741001000111 Dysplasie, mesomele, Typ Nievergelt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4500341000241112 dysplasie mésomélique de type Nievergelt fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4500341000241112 dysplasie mésomélique de type Nievergelt fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391741001000111 Dysplasie, mesomele, Typ Nievergelt 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
Nievergelt's syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Is a Mesomelic dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Is a Congenital anomaly of skeletal bone false Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Clinical course Progressive false Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Interprets Height / growth measure (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Nievergelt's syndrome Interprets Limb length true Inferred relationship Existential restriction modifier (core metadata concept) 3
Nievergelt's syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Nievergelt's syndrome Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier (core metadata concept) 1
Nievergelt's syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Is a Congenital abnormal shape of fibula (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Is a Congenital abnormal shape of tibia true Inferred relationship Existential restriction modifier (core metadata concept)
Nievergelt's syndrome Finding site Bone structure of tibia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Associated morphology Abnormal shape (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Nievergelt's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Nievergelt's syndrome Finding site Bone structure of fibula true Inferred relationship Existential restriction modifier (core metadata concept) 4
Nievergelt's syndrome Associated morphology Abnormal shape (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Nievergelt's syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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