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105840005: Iron AND/OR iron compound (substance)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Jern OG/ELLER jernforbindelse	Is a	Metal OG/ELLER metalforbindelse	false	Inferred relationship	Some
Jern OG/ELLER jernforbindelse	Is a	Allergen class	false	Inferred relationship	Some
Jern OG/ELLER jernforbindelse	Is a	Drug allergen	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Ferrocyanide salt	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Iron	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Iron compound	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Siderosis of cornea	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Sodium ferric gluconate complex	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Iron sucrose	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Ferumoxide (substance)	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Ferumoxsil (substance)	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Iron	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Focal hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Hemosiderosis, acquired	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Hereditary hemochromatosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Secondary hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Idiopathic pulmonary hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
The early-onset and most severe form of hereditary hemochromatosis a group of diseases characterized by excessive tissue iron deposition of genetic origin. This juvenile form of hemochromatosis has the classical features of HH but is also characterized by severe cardiomyopathy and hypogonadism. Arthropathy, hepatic fibrosis, glucose intolerance, and increased skin pigmentation are frequent. Two types of the disease have been described, both being transmitted in an autosomal recessive way.	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Secondary hemochromatosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Iron overload	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Neonatal hemochromatosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
African nutritional hemochromatosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Transfusion hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Shunt hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Erythropoietic hemochromatosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Renal hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Hepatic hemosiderosis	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Idiopathic hemochromatosis (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
hæmosiderose med levercirrose	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Bronze diabetes (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Primary hemochromatosis (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Hemochromatosis (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Sphalerite (substance)	Is a	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Poisoning caused by iron and/or iron compound (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Neuroferritinopathy (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Milk-induced pulmonary disease in infant	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Hemochromatosis following repeated red blood cell transfusion	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Secondary pulmonary hemosiderosis is a respiratory disease due to the deposition of hemosiderin-laden macrophages in lungs as a result of repeated alveolar hemorrhage secondary to another disease, especially dysimmunitary disorders (i.e. Heiner syndrome, autoimmune diseases), thrombotic disorders and cardiovascular disorders such as mitral stenosis. It manifests as a triad of hemoptysis, anemia and diffuse parenchymal infiltrates on chest radiography.	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
A form of rare hemochromatosis (HC) characterized by excessive tissue iron deposition of genetic origin and presenting with liver disease, hypogonadism, arthritis, diabetes and skin pigmentation.	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
Autosomal dominant hereditary hemochromatosis (disorder)	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some
COASY protein-associated neurodegeneration (CoPAN) is a very rare, slowly progressive form of neurodegeneration with brain iron accumulation (NBIA) characterized by classic NBIA features. The clinical manifestations include early-onset spastic-dystonic paraparesis, oromandibular dystonia, dysarthria, parkinsonism, axonal neuropathy, progressive cognitive impairment, complex motor tics, and obsessive-compulsive disorder.	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some	1
Beta-propeller protein-associated neurodegeneration (BPAN), also known as static encephalopathy of childhood with neurodegeneration in adulthood, is a rare form of neurodegeneration with brain iron accumulation (NBIA) characterized by early-onset developmental delay and further neurological deterioration in early adulthood.	Causative agent	False	Jern OG/ELLER jernforbindelse	Inferred relationship	Some	1

Reference Sets

Concept inactivation indicator reference set

US English

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Id	Description	Lang	Type	Status	Case?	Module
170253014	Iron AND/OR iron compound	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
575548012	Iron AND/OR iron compound (substance)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1219170010	Iron and its derivatives	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2855811000005115	Jern OG/ELLER jernforbindelse	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)