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254092004: Saldino-Mainzer dysplasia (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
378248015 Saldino-Mainzer dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
644936017 Saldino-Mainzer dysplasia (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2966749018 Conorenal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3788779012 Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378247013 Renal dysplasia, retinal pigmentory dystrophy, cerebellar ataxia and skeletal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378247013 Renal dysplasia, retinal pigmentory dystrophy, cerebellar ataxia and skeletal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378248015 Saldino-Mainzer dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
644936017 Saldino-Mainzer dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644936017 Saldino-Mainzer dysplasia (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2966749018 Conorenal syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2966749018 Conorenal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3788779012 Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3386211001000110 Saldino-Mainzer-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5081741000241110 dysplasie de Saldino-Mainzer fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5081741000241110 dysplasie de Saldino-Mainzer fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386211001000110 Saldino-Mainzer-Syndrom 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
Saldino-Mainzer dysplasia Is a Acromesomelic dysplasia group (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Is a Disorder of limb false Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Saldino-Mainzer dysplasia Finding site Kidney structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Saldino-Mainzer dysplasia Is a Renal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Saldino-Mainzer dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 3
Saldino-Mainzer dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Saldino-Mainzer dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Saldino-Mainzer dysplasia Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
Saldino-Mainzer dysplasia Finding site Kidney structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Saldino-Mainzer dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Saldino-Mainzer dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Finding site Kidney structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Saldino-Mainzer dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Saldino-Mainzer dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Saldino-Mainzer dysplasia Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Saldino-Mainzer dysplasia Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Saldino-Mainzer dysplasia Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Hereditary nephropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Hereditary ataxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Skeletal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Finding site Structure of retinal pigment epithelium true Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Retinal pigment epithelial dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Saldino-Mainzer dysplasia Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Saldino-Mainzer dysplasia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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