(Q56013953)

English

familial progressive hyper- and hypopigmentation

human disease

FPHH
familial progressive hyperpigmentation with or without hypopigmentation

In more languages

default values for all languages

No label defined

No description defined

Statements

class of disease

0 references

autosomal dominant disease

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

familial progressive hyperpigmentation

0 references

http://www.orpha.net/ORDO/Orphanet_280628

0 references

http://purl.obolibrary.org/obo/DOID_0111373

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0111373

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

24 November 2020

Disease Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

ICD-11 ID (Foundation)

0 references

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

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

Sitelinks

Wikipedia(0 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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