(Q56013962)

English

facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion

human disease

Deletion 10p11.21p12.31
10p12p11 microdeletion syndrome
Del(10)(p11.21p12.31)
Monosomy 10p11.21p12.31

In more languages

Statements

class of disease

0 references

http://www.orpha.net/ORDO/Orphanet_284169

0 references

Identifiers

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

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q56013962&oldid=2088119140"