FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

1162852008: Familial normophosphatemic tumoral calcinosis (disorder)


Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4591770013 Normocalcaemic tumoural calcinosis en Synonym Active Case insensitive SNOMED CT core
4591771012 Normocalcemic tumoral calcinosis en Synonym Active Case insensitive SNOMED CT core
4591776019 Familial normophosphatemic tumoral calcinosis en Synonym Active Case insensitive SNOMED CT core
4591778018 Familial normophosphatemic tumoral calcinosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4591922012 Familial normophosphataemic tumoural calcinosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial normophosphataemic tumoural calcinosis Is a Tumoural calcinosis true Inferred relationship Some
Familial normophosphataemic tumoural calcinosis Associated morphology Dystrophic calcification true Inferred relationship Some 1
Familial normophosphataemic tumoural calcinosis Finding site Structure of joint region true Inferred relationship Some 2
Familial normophosphataemic tumoural calcinosis Associated morphology Dystrophic calcification true Inferred relationship Some 2
Familial normophosphataemic tumoural calcinosis Finding site Skin structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start