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860796007: Hyperphosphatemic familial tumoral calcinosis (disorder)


Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3944205013 Hyperphosphataemic familial tumoural calcinosis en Synonym Active Case insensitive SNOMED CT core
3944206014 Hyperphosphatemic familial tumoral calcinosis en Synonym Active Case insensitive SNOMED CT core
3944207017 Hyperphosphatemic familial tumoral calcinosis (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
Hyperphosphataemic familial tumoural calcinosis Is a Tumoural calcinosis true Inferred relationship Some
Hyperphosphataemic familial tumoural calcinosis Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Hyperphosphataemic familial tumoural calcinosis Is a Hereditary disorder of the integument false Inferred relationship Some
Hyperphosphataemic familial tumoural calcinosis Associated morphology Dystrophic calcification true Inferred relationship Some 1
Hyperphosphataemic familial tumoural calcinosis Finding site Skin structure true Inferred relationship Some 1
Hyperphosphataemic familial tumoural calcinosis Associated morphology Pathologic calcification false Inferred relationship Some 2
Hyperphosphataemic familial tumoural calcinosis Finding site Subcutaneous tissue structure false Inferred relationship Some 2
Hyperphosphataemic familial tumoural calcinosis Finding site Structure of joint region true Inferred relationship Some 2
Hyperphosphataemic familial tumoural calcinosis Associated morphology Dystrophic calcification true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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