(Q7662637)

English

synpolydactyly

syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene

syndactyly type 2
Synpolydactyly

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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

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1 reference

30 November 2020

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dysostosis of genetic origin with limb anomaly as a major feature

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly

HOXD13

1 reference

stated in

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

on focus list of Wikimedia project

WikiProject Medicine

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NCI Thesaurus ID

C75005

1 reference

28 August 2019

C75003

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28 August 2019

http://purl.obolibrary.org/obo/DOID_0060242

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30 November 2020

http://identifiers.org/doid/DOID:0060242

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_295195

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Identifiers

MeSH descriptor ID

C538153

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

28 August 2019

0 references

1 reference

1 reference

30 November 2020

1 reference

imported from Wikimedia project

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28 August 2019

Microsoft Academic ID

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1 reference

28 August 2019

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28 August 2019

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28 August 2019

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28 August 2019

1 reference

28 August 2019

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Wikipedia(1 entry)

enwiki Synpolydactyly

(Q7662637)

synpolydactyly

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