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782785002: X-linked osteoporosis with fractures (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3755754019 X-linked osteoporosis with fractures en Synonym Active Entire term case sensitive SNOMED CT core module
3755755018 X-linked osteoporosis with fractures (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked osteoporosis with fractures Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
X-linked osteoporosis with fractures Is a Dysplasia with decreased bone density true Inferred relationship Existential restriction modifier
X-linked osteoporosis with fractures Finding site Bone structure true Inferred relationship Existential restriction modifier 1
X-linked osteoporosis with fractures Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
X-linked osteoporosis with fractures Occurrence Congenital true Inferred relationship Existential restriction modifier 1
X-linked osteoporosis with fractures Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked osteoporosis with fractures Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
X-linked osteoporosis with fractures Interprets Bone density scan true Inferred relationship Existential restriction modifier 2
X-linked osteoporosis with fractures Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
X-linked osteoporosis with fractures Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
X-linked osteoporosis with fractures Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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