123768009: Hereditary methemoglobinemia, enzymatic type (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

192257013 Hereditary methemoglobinemia, enzymatic type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

203424018 Hereditary methaemoglobinaemia, enzymatic type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

726848012 Hereditary methemoglobinemia, enzymatic type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

192257013 Hereditary methemoglobinemia, enzymatic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

192257013 Hereditary methemoglobinemia, enzymatic type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

203424018 Hereditary methaemoglobinaemia, enzymatic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

203424018 Hereditary methaemoglobinaemia, enzymatic type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

726848012 Hereditary methemoglobinemia, enzymatic type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

726848012 Hereditary methemoglobinemia, enzymatic type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary methemoglobinemia, enzymatic type	Is a	Inborn error of metabolism	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Hereditary disorder of haematologic sysem	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Enzymopathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Methemoglobinemia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Congenital anomaly of the haematopoietic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Has definitional manifestation	Red blood cell finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Congenital methemoglobinemia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	Hereditary red blood cell disorder (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cytochrome b>3< deficiency	Is a	False	Hereditary methemoglobinemia, enzymatic type	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methemoglobin reductase deficiency (disorder)	Is a	False	Hereditary methemoglobinemia, enzymatic type	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

REPLACED BY association reference set (foundation metadata concept)