Details of Disease | DrugMAP

General Information of Disease (ID: DISVZ41G)

Disease Name	L-ferritin deficiency
Synonyms	LFTD; L-ferritin deficiency, dominant and recessive; L-ferritin deficiency
Disease Hierarchy	DISYKSRF: Genetic disease DIS9XD9A: Hematologic disease DISVZ41G: L-ferritin deficiency
Disease Identifiers	MONDO ID MONDO_0014274 UMLS CUI C3810090 OMIM ID 615604 MedGen ID 816420 Orphanet ID 440731 SNOMED CT ID 1217208003

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
FTL	OTYQA8A6	Strong	Autosomal dominant	[1]
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References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.