(Q32146937)

English

Fanconi anemia complementation group G

human disease

FANCG
Fanconi anemia complementation group type G
Fanconi Anemia, Complementation Group type G
FANCONI ANEMIA, COMPLEMENTATION GROUP G
FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG

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Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

0 references

1 reference

29 November 2020

1 reference

15 May 2019

1 reference

29 November 2020

4 references

13 August 2019

The Fanconi anaemia group G gene FANCG is identical with XRCC9

8 December 2020

https://search.clinicalgenome.org/kb/gene-validity/1913bd10-1355-4067-93b6-9068924d77df--2019-04-19T16:00:00

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_1913bd10-1355-4067-93b6-9068924d77df-2018-12-21T151935.075Z

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C125708

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://purl.obolibrary.org/obo/DOID_0111086

1 reference

29 November 2020

http://identifiers.org/doid/DOID:0111086

2 references

10 July 2020

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

Identifiers

1 reference

29 November 2020

0 references

1 reference

28 August 2019

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

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