Genopathy
Gene-Disorder Association · Article
Gene
CDAN1
Codanin 1
Disorder
Protein-Deficiency Anemia
First reported 2008
Supporting publications 1
Key publication · gene–disorder Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1).European journal of haematology · 2008
Key publication · disorder State of haemoglobin in sickle-cell anaemia.Nature · 1950
Manually curated
Association Review

In brief

The association between CDAN1 (Codanin 1) and Protein-Deficiency Anemia is reported, with clinical genetic testing available.

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

Association overview

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

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
CDAN1

The gene

1 source summary

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

Request access
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).

Request access
05
Literature

Reading

1 publication

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Request access
06
Provenance

References & sources

4 references

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

Request access