(Q1437472)

English

atransferrinemia

Human disease

familial hypotransferrinemia
Congenital hypotransferrinemia
Transferrin Serum Level Quantitative Trait Locus 1
Congenital Atransferrinemia
ATRANSFERRINEMIA
Hereditary Atransferrinemia
Hypotransferrinemia, Familial

In more languages

default for all languages

No label defined

No description defined

Statements

0 references

class of disease

0 references

metal metabolism disorder

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

constitutional anemia due to iron metabolism disorder

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

3 references

UniProt protein ID

13 August 2019

Molecular characterization of a case of atransferrinemia

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000091513/MONDO_0008846

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C125693

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

C125693

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_0050649

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:0050649

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

http://purl.obolibrary.org/obo/HP_0012239

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

http://www.orpha.net/ORDO/Orphanet_1195

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

0 references

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

imported from Wikimedia project

English Wikipedia

GARD rare disease ID

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

Disease Ontology

28 August 2019

Disease Ontology ID

Human Phenotype Ontology ID

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 ID (Foundation)

0 references

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

0 references

0 references

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

Disease Ontology

28 August 2019

Disease Ontology ID

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

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

UniProt disease ID

0 references

WikiProjectMed ID

Atransferrinemia

0 references

Sitelinks

Wikipedia(5 entries)

bswiki Atransferinemija
dewiki Hereditäre Atransferrinämie und Hypotransferrinämie
enwiki Atransferrinemia
hrwiki Atransferinemija
srwiki Атрансферинемија

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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