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389191003: Osteoplastic dysplasia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1463370014 Osteoplastic dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1483243014 Osteoplastic dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1463370014 Osteoplastic dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1463370014 Osteoplastic dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1483243014 Osteoplastic dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1483243014 Osteoplastic dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5246741000241117 dysplasie ostéoplastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5246741000241117 dysplasie ostéoplastique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteoplastic dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Is a Skeletal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Osteoplastic dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Osteoplastic dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Osteoplastic dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Osteoplastic dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Osteoplastic dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteoplastic dysplasia Finding site Skeletal system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Osteodysplastic dysplasia, type I (disorder) Is a True Osteoplastic dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Osteodysplastic dysplasia, type II Is a True Osteoplastic dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
dysplasie ostéodysplasique microcéphalique type Saul-Wilson Is a False Osteoplastic dysplasia Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type is a skeletal dysplasia characterised by a distinct facial phenotype, short stature, brachydactyly, clubfoot deformities, cataracts, and microcephaly. It has been described in four patients. Facial features include frontal bossing with a depression over the metopic suture, a narrow nasal root with a beaked nose, and midfacial hypoplasia with prominent eyes. Characteristic radiographic findings are observed (irregularities of the vertebral bodies, hypoplasia of the odontoid process, short phalanges, coning several epiphyses etc.). Is a True Osteoplastic dysplasia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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