(Q7180213)

English

Phakomatosis pigmentovascularis

human disease

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

class of disease

0 references

hyperpigmentation

0 references

malformation syndrome with hamartosis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

syndromic glaucoma

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

syndromic developmental defect of the eye

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

hyperpigmentation of the skin

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

709.09

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_2875

0 references

Identifiers

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 (foundation)

0 references

Microsoft Academic ID

0 references

0 references

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

WikiProjectMed ID

Phakomatosis pigmentovascularis

0 references

Sitelinks

Wikipedia(1 entry)

enwiki Phakomatosis pigmentovascularis

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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