FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

105985007: Osteochondrodysplasia syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
170404011 Osteochondrodysplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
576952012 Osteochondrodysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

54 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteochondrodysplasia syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Osteochondrodysplasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Osteochondrodysplasia syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Osteochondrodysplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Osteochondrodysplasia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Osteochondrodysplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Osteochondrodysplasia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Kozlowski spondylometaphyseal dysplasia Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Autosomal recessive spondyloepimetaphyseal dysplasia Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Dysplasias with significant membranous bone involvement Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia with joint laxity Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Osteodysplastic primordial dwarfism Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Kniest-Stickler dysplasia group Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Metatropic dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Metaphyseal chondrodysplasia, Jansen type Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Thanatophoric dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Diaphyseal dysplasia Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Craniometaphyseal dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Spondyloepiphyseal dysplasia congenita Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Atelosteogenesis Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Spondyloepiphyseal dysplasia tarda Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Chondroectodermal dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Frontometaphyseal dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Hajdu-Cheney syndrome Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Kenny syndrome Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Neonatal osteosclerotic dysplasia Is a False Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Spondyloperipheral dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Spondyloepimetaphyseal dysplasia, Strudwick type Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Spondylocarpotarsal synostosis syndrome Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Kniest-Stickler dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Kniest dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Lethal Kniest-like syndrome Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Otospondylomegaepiphyseal dysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier
Complex lethal osteochondrodysplasia Is a True Osteochondrodysplasia syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start