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205483007: Hypochondrogenesis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
315102015 Hypochondrogenesis en Synonym Active Case insensitive SNOMED CT core
590856010 Hypochondrogenesis (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
Hypochondrogenesis Pathological process Pathological developmental process true Inferred relationship Some 1
Hypochondrogenesis Occurrence Congenital true Inferred relationship Some 1
Hypochondrogenesis Associated morphology Congenital dysplasia false Inferred relationship Some 1
Hypochondrogenesis Is a Spondyloepiphyseal dysplasia congenita true Inferred relationship Some
Hypochondrogenesis Associated morphology Congenital dysplasia false Inferred relationship Some 1
Hypochondrogenesis Finding site Bone structure false Inferred relationship Some 1
Hypochondrogenesis Associated morphology Dysplasia true Inferred relationship Some 1
Hypochondrogenesis Finding site Bone structure true Inferred relationship Some 1
Hypochondrogenesis Occurrence Congenital false Inferred relationship Some
Hypochondrogenesis Finding site Skeletal system structure false Inferred relationship Some 1
Hypochondrogenesis Occurrence Congenital false Inferred relationship Some 2
Hypochondrogenesis Finding site Bone structure false Inferred relationship Some 2
Hypochondrogenesis Associated morphology Congenital dysplasia false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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