pentasomy X

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sex chromosome aneuploidy where a female has three additional X chromosomes

External resources

Freebase ID	/m/0b1wfk^[1]
Microsoft Academic ID	2780328832
Google Knowledge Graph ID	/g/121hxj4s
ICD-10-CM	Q97.1^[2]
GARD rare disease ID	5678^[3]
UMLS CUI	C2937419^[2] mapping relation type: close match C0265497^[2] mapping relation type: përputhje e përpiktë
Miraheze article ID	lgbta:Pentasomy_X mogai:Pentasomy_X
ICD-10	Q97.1
DiseasesDB	32625
ICD-11 ID (Foundation)	2087864894
APA Dictionary of Psychology entry	xxxxx-syndrome
Orphanet ID	11^[2] mapping relation type: përputhje e përpiktë
WikiProjectMed ID	Pentasomy X
MeSH descriptor ID	C535319^[2] mapping relation type: përputhje e përpiktë
Mondo ID	MONDO_0015228

rare disease

chromosomal disease

developmental defect during embryogenesis^[2]

class of disease

sex chromosome disorder

Polysomy of X chromosome^[2]

women's health

medical genetics

gender gap on Dutch Wikipedia

A90

C89802^[2]

mapping relation type: përputhje e përpiktë

Pentasomy X

^ Freebase Data Dumps, 28 tetor 2013
^ ^a ^b ^c ^d ^e ^f ^g ^h Monarch Disease Ontology release 2018-06-29, 28 korrik 2018, MONDO_0015228
^ Genetic and Rare Diseases Information Center, 29 mars 2019