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86470003: Osteogenesis imperfecta, recessive perinatal lethal (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
143392014 Osteogenesis imperfecta, recessive perinatal lethal en Synonym Active Case insensitive SNOMED CT core
143393016 Vrolik disease en Synonym Active Case sensitive SNOMED CT core
143394010 Osteogenesis imperfecta, type II, recessive form en Synonym Active Initial character case insensitive SNOMED CT core
143395011 Porak-Durante syndrome en Synonym Active Case sensitive SNOMED CT core
143396012 Osteogenesis imperfecta, Vrolik type en Synonym Active Initial character case insensitive SNOMED CT core
828740016 Osteogenesis imperfecta, recessive perinatal lethal (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta, recessive perinatal lethal Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal Pathological process 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
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 Is a Fragilitas ossium congenita false 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 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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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