FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

86470003: Osteogenesis imperfecta, recessive perinatal lethal (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
143392014 Osteogenesis imperfecta, recessive perinatal lethal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
143393016 Vrolik disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
143394010 Osteogenesis imperfecta, type II, recessive form en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
143395011 Porak-Durante syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
143396012 Osteogenesis imperfecta, Vrolik type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
828740016 Osteogenesis imperfecta, recessive perinatal lethal (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta, recessive perinatal lethal Is a Osteogenesis imperfecta, perinatal lethal (disorder) false Inferred relationship Some
Osteogenesis imperfecta, recessive perinatal lethal Finding site Bone structure true Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Occurrence Congenital false Inferred relationship Some
Osteogenesis imperfecta, recessive perinatal lethal Finding site Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Associated morphology Dysplasia true Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Finding site Connective tissue false Inferred relationship Some
Osteogenesis imperfecta, recessive perinatal lethal Finding site Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta, recessive perinatal lethal Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Is a Osteogenesis imperfecta, perinatal lethal true Inferred relationship Some
Osteogenesis imperfecta, recessive perinatal lethal Finding site Bone structure false Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Occurrence Congenital false Inferred relationship Some 2
Osteogenesis imperfecta, recessive perinatal lethal Finding site Bone structure false Inferred relationship Some 2
Osteogenesis imperfecta, recessive perinatal lethal Associated morphology Congenital dysplasia false Inferred relationship Some 2
Osteogenesis imperfecta, recessive perinatal lethal Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Has interpretation Abnormal true Inferred relationship Some 2
Osteogenesis imperfecta, recessive perinatal lethal Interprets Bone formation true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts Is a False Osteogenesis imperfecta, recessive perinatal lethal Inferred relationship Some

This concept is not in any reference sets

Back to Start