X Chromosome, Trisomy Xp3 - Ontology Report

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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:	X Chromosome, Trisomy Xp3	go back to main search page
Accession:	DOID:9000833	browse the term
Synonyms:	exact_synonym:	Duplication Xp3; Trisomy Xp3
	primary_id:	MESH:C536756; RDO:0002436

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0 Annotations Found

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Term paths to the root

Path 1
Term	Annotations
disease	21089
syndrome	10784
chromosomal duplication syndrome	1259
Trisomy	369
X Chromosome, Trisomy Xp3	0
Path 2
Term	Annotations
disease	21089
Developmental Disease	18391
Congenital, Hereditary, and Neonatal Diseases and Abnormalities	18246
Congenital Abnormalities	7506
chromosomal disease	2827
chromosomal duplication syndrome	1259
Trisomy	369
X Chromosome, Trisomy Xp3	0

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RGD DISEASE ONTOLOGY - ANNOTATIONS