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771445001: Autosomal recessive infantile hypercalcemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3706227018 Autosomal recessive infantile hypercalcemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3706228011 Autosomal recessive infantile hypercalcaemia en Synonym Active Entire term case insensitive SNOMED CT core module
3706229015 Familial infantile hypercalcaemia with suppressed intact parathyroid hormone en Synonym Active Entire term case insensitive SNOMED CT core module
3706230013 Autosomal recessive infantile hypercalcemia en Synonym Active Entire term case insensitive SNOMED CT core module
3706231012 Familial infantile hypercalcemia with suppressed intact parathyroid hormone 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
Autosomal recessive infantile hypercalcemia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive infantile hypercalcemia Is a Infantile hypercalcemia true Inferred relationship Existential restriction modifier
Autosomal recessive infantile hypercalcemia Has interpretation Above reference range true Inferred relationship Existential restriction modifier 1
Autosomal recessive infantile hypercalcemia Interprets Serum calcium measurement true Inferred relationship Existential restriction modifier 1
Autosomal recessive infantile hypercalcemia Occurrence Infancy 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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