(Q55784762)

English

L-ferritin deficiency

human disease

LFTD
L-FERRITIN DEFICIENCY; LFTD
L-FERRITIN DEFICIENCY

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Statements

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class of disease

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genetic hematologic disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

1 reference

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

http://www.orpha.net/ORDO/Orphanet_440731

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Identifiers

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

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