(Q5026799)

English

Camisa disease

medical condition

Keratoderma hereditarium mutilans with ichthyosis
Mutilating Keratoderma With Ichthyosis
Keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome
VOHWINKEL SYNDROME, VARIANT FORM
Vohwinkel Syndrome With Ichthyosis
Loricrin Keratoderma

In more languages

Statements

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class of disease

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Vohwinkel syndrome

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inherited non-syndromic ichthyosis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

autosomal dominant diffuse mutilating palmoplantar keratoderma

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic association

1 reference

A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome

http://www.orpha.net/ORDO/Orphanet_79395

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Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Microsoft Academic ID

0 references

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mapping relation type

2 references

imported from Wikimedia project

English Wikipedia

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

UniProt disease ID

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WikiProjectMed ID

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Sitelinks

Wikipedia(2 entries)

enwiki Camisa disease
itwiki Cheratodermia da loricrina

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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