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

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

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