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55236002: Infantile hypophosphatasia (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
91833019 Infantile hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91834013 Hypophosphatasia, infantile type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91835014 Congenital hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91836010 Fetal hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
497162013 Phosphoethanolaminuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
497163015 Rathbun syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
793556018 Infantile hypophosphatasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3012196012 Foetal hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91833019 Infantile hypophosphatasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
91833019 Infantile hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91834013 Hypophosphatasia, infantile type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
91834013 Hypophosphatasia, infantile type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91835014 Congenital hypophosphatasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
91835014 Congenital hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
91836010 Fetal hypophosphatasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
91836010 Fetal hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
497162013 Phosphoethanolaminuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
497162013 Phosphoethanolaminuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
497163015 Rathbun syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
793556018 Infantile hypophosphatasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
793556018 Infantile hypophosphatasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3012196012 Foetal hypophosphatasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3012196012 Foetal hypophosphatasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3422091001000111 Hypophosphatasie, infantile de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
891191000172110 hypophosphatasie infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1009431000172116 maladie de Rathburn infantile fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
891191000172110 hypophosphatasie infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1009431000172116 maladie de Rathburn infantile fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3422091001000111 Hypophosphatasie, infantile de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile hypophosphatasia (disorder) Is a Enzymopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile hypophosphatasia (disorder) Is a Hypophosphatasia true Inferred relationship Existential restriction modifier (core metadata concept)
Infantile hypophosphatasia (disorder) Is a Autosomal hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile hypophosphatasia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile hypophosphatasia (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Infantile hypophosphatasia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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