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86470003: recessieve osteogenesis imperfecta type II (aandoening)


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
6875961000146118 recessieve osteogenesis imperfecta type II nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6876051000146111 recessieve perinatale letale osteogenesis imperfecta nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7331681000146119 recessieve osteogenesis imperfecta type 2 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13584101000146119 recessieve osteogenesis imperfecta type II (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


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 congenitale dysplasie (afwijkende morfologie) 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 congenitale dysplasie (afwijkende morfologie) 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 congenitale dysplasie (afwijkende morfologie) 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

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