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890437007: Chondrodysplasia punctata due to maternal autoimmune disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4012567011 Chondrodysplasia punctata due to maternal autoimmune disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4012568018 Chondrodysplasia punctata due to maternal autoimmune disease en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chondrodysplasia punctata due to maternal autoimmune disease Is a Chondrodysplasia punctata true Inferred relationship Existential restriction modifier
Chondrodysplasia punctata due to maternal autoimmune disease Causative agent Autoantibody true Inferred relationship Existential restriction modifier 1
Chondrodysplasia punctata due to maternal autoimmune disease Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Chondrodysplasia punctata due to maternal autoimmune disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chondrodysplasia punctata due to maternal autoimmune disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Chondrodysplasia punctata due to maternal autoimmune disease Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Chondrodysplasia punctata due to maternal autoimmune disease Due to Autoimmune disease true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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