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55236002: Infantile hypophosphatasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
91833019 Infantile hypophosphatasia en Synonym Active Entire term case insensitive SNOMED CT core module
91834013 Hypophosphatasia, infantile type en Synonym Active Entire term case insensitive SNOMED CT core module
91835014 Congenital hypophosphatasia en Synonym Active Entire term case insensitive SNOMED CT core module
91836010 Fetal hypophosphatasia en Synonym Active Entire term case insensitive SNOMED CT core module
497162013 Phosphoethanolaminuria en Synonym Active Entire term case insensitive SNOMED CT core module
497163015 Rathbun syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
793556018 Infantile hypophosphatasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3012196012 Foetal hypophosphatasia 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
Infantile hypophosphatasia Is a Enzymopathy true Inferred relationship Existential restriction modifier
Infantile hypophosphatasia Is a Hypophosphatasia true Inferred relationship Existential restriction modifier
Infantile hypophosphatasia Is a Autosomal hereditary disorder false Inferred relationship Existential restriction modifier
Infantile hypophosphatasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Infantile hypophosphatasia Finding site Body system structure false Inferred relationship Existential restriction modifier
Infantile hypophosphatasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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