Disease #00210 (PCS (PREMATURE CHROMATID SEPARATION TRAIT), OMIM:176430)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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	Curator: Florian Bayersdorfer

Official abbreviation	PCS
Name	PREMATURE CHROMATID SEPARATION TRAIT
OMIM ID	176430
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BUB1B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-07-29 06:49:06 +00:00 (UTC)
Date last edited	N/A