(Q5160422)

English

congenital dyserythropoietic anemia

congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood

congenital dyshaematopoietic anaemia
CDA

In more languages

Statements

designated intractable/rare disease

1 reference

https://ddrare.nibiohn.go.jp/

17 May 2019

0 references

class of disease

0 references

congenital hemolytic anemia

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

ineffective erythropoiesis

2 references

Congenital Dyserythropoietic Anemia Type 1: Report of One Patient and Analysis of Previously Reported Patients Treated with Interferon Alpha

Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations.

constitutional dyserythropoietic anemia

0 references

health specialty

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genetic association

1 reference

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I

1 reference

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

external data available at URL

http://www.nanbyou.or.jp/entry/4363

language of work or name

1 reference

https://ddrare.nibiohn.go.jp/

17 May 2019

on focus list of Wikimedia project

WikiProject Medicine

0 references

285.8

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

NCI Thesaurus ID

C84646

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

C84646

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

http://purl.obolibrary.org/obo/DOID_1338

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:1338

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

http://www.orpha.net/ORDO/Orphanet_85

0 references

Identifiers

MeSH descriptor ID

mapping relation type

subject named as

Anemia, Dyserythropoietic, Congenital

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

C15.378.071.141.150.095

0 references

C16.320.070.095

0 references

0 references

1 reference

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

GARD rare disease ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

Genetics Home Reference Conditions ID

congenital-dyserythropoietic-anemia

0 references

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

7 August 2018

ICD-11 (foundation)

0 references

ICD-11 ID (MMS)

3A73

subject named as

Congenital dyserythropoietic anaemia

0 references

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

0 references

0 references

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

Sitelinks

Wikipedia(5 entries)

arwiki فقر الدم بخلل تكون الكريات الحمر الخلقي
dewiki Kongenitale Dyserythropoetische Anämie
enwiki Congenital dyserythropoietic anemia
jawiki 先天性赤血球異形成貧血
zh_yuewiki 先天性紅血球生成性貧血

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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