(Q5432946)

English

familial progressive hyperpigmentation

medical condition

Fph
Melanosis universalis hereditaria
HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1
HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1; FPH1
FPH1
Melanosis diffusa congenita
Universal melanosis

In more languages

Statements

0 references

class of disease

0 references

pigmentation disorder

0 references

genetic association

1 reference

Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation

http://www.orpha.net/ORDO/Orphanet_79146

0 references

Identifiers

0 references

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

ICD-11 (foundation)

0 references

Microsoft Academic ID

0 references

0 references

0 references

0 references

0 references

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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

UniProt disease ID

0 references

WikiProjectMed ID

Familial progressive hyperpigmentation

0 references

Sitelinks

Wikipedia(3 entries)

enwiki Familial progressive hyperpigmentation
eswiki Hiperpigmentación progresiva familiar
itwiki Iperpigmentazione familiare progressiva

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q5432946&oldid=2087140983"