FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

124678007: Deficiency of bisphosphoglycerate mutase (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
204933019 Deficiency of glycerate phosphomutase en Synonym Active Entire term case insensitive SNOMED CT core module
204934013 Deficiency of diphosphoglycerate mutase en Synonym Active Entire term case insensitive SNOMED CT core module
204935014 Deficiency of bisphosphoglycerate synthase en Synonym Active Entire term case insensitive SNOMED CT core module
204936010 Deficiency of bisphosphoglycerate mutase en Synonym Active Entire term case insensitive SNOMED CT core module
728405015 Deficiency of bisphosphoglycerate mutase (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of bisphosphoglycerate mutase Is a Specific enzyme deficiency true Inferred relationship Existential restriction modifier
Deficiency of bisphosphoglycerate mutase Finding site Body system structure false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency Is a False Deficiency of bisphosphoglycerate mutase Inferred relationship Existential restriction modifier
Familial erythrocytosis due to diphosphoglycerate mutase deficiency Associated etiologic finding False Deficiency of bisphosphoglycerate mutase Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency Associated etiologic finding False Deficiency of bisphosphoglycerate mutase Inferred relationship Existential restriction modifier
Familial erythrocytosis due to diphosphoglycerate mutase deficiency Due to True Deficiency of bisphosphoglycerate mutase Inferred relationship Existential restriction modifier 2
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency Due to True Deficiency of bisphosphoglycerate mutase Inferred relationship Existential restriction modifier 5

This concept is not in any reference sets

Back to Start