Genopathy
Gene-Disorder Association · Article
Gene
FECH
Ferrochelatase
Disorder
Protein-Deficiency Anemia
First reported 1991
Key publication · gene–disorder Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.The Journal of clinical investigation · 1991
Key publication · disorder State of haemoglobin in sickle-cell anaemia.Nature · 1950
Manually curated
Association Review

In brief

The association between FECH (Ferrochelatase) and Protein-Deficiency Anemia is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
FECH

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Protein-Deficiency Anemia

The disorder

20 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Provenance

References & sources

3 references

Every source and publication cited across this dossier, as one numbered reference list.

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