237916000: Fumarylacetoacetase deficiency (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

356575017 Fumarylacetoacetase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

356576016 Tyrosinaemia type I en Synonym Active Only initial character case insensitive SNOMED CT core module

356577013 Hereditary tyrosinemia type I en Synonym Active Only initial character case insensitive SNOMED CT core module

356578015 Hereditary tyrosinaemia type I en Synonym Active Only initial character case insensitive SNOMED CT core module

356579011 Tyrosinemia type I en Synonym Active Only initial character case insensitive SNOMED CT core module

626716015 Fumarylacetoacetase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Fumarylacetoacetase deficiency	Is a	Hereditary hypertyrosinemia	false	Inferred relationship	Existential restriction modifier
Fumarylacetoacetase deficiency	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Fumarylacetoacetase deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fumarylacetoacetase deficiency, acute type	Is a	False	Fumarylacetoacetase deficiency	Inferred relationship	Existential restriction modifier
Fumarylacetoacetase deficiency, chronic type	Is a	False	Fumarylacetoacetase deficiency	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets