(Q3042143)

English

frontometaphyseal dysplasia

human disease

FMD
FMD1
FRONTOMETAPHYSEAL DYSPLASIA 1; FMD1

In more languages

Statements

hereditary disorder

0 references

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class of disease

0 references

otopalatodigital syndrome spectrum disorder

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

health specialty

medical genetics

0 references

genetic association

2 references

UniProt protein ID

13 August 2019

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

http://purl.obolibrary.org/obo/DOID_0111785

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0111785

1 reference

Identifiers.org

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

Identifiers

MeSH descriptor ID

0 references

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Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

GARD rare disease ID

0 references

Genetics Home Reference Conditions ID

frontometaphyseal-dysplasia

0 references

0 references

0 references

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

Sitelinks

Wikipedia(3 entries)

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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