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1162808000: Familial calcium pyrophosphate dihydrate crystal deposition disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4591530015 Familial calcium pyrophosphate dihydrate crystal deposition disease en Synonym Active Entire term case insensitive SNOMED CT core module
4591531016 Familial calcium pyrophosphate dihydrate crystal deposition disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4591536014 Familial calcium pyrophosphate deposition disease en Synonym Active Entire term case insensitive SNOMED CT core module
4591537017 Familial CPPD (calcium pyrophosphate deposition disease) en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial calcium pyrophosphate dihydrate crystal deposition disease Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial calcium pyrophosphate dihydrate crystal deposition disease Is a Calcium pyrophosphate deposition disease true Inferred relationship Existential restriction modifier
Familial calcium pyrophosphate dihydrate crystal deposition disease Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Familial calcium pyrophosphate dihydrate crystal deposition disease Finding site Joint structure true Inferred relationship Existential restriction modifier 1
Familial calcium pyrophosphate dihydrate crystal deposition disease Associated morphology Deposition of calcium pyrophosphate crystals, calcified structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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