Disease #00101 (MMRCS2 (MISMATCH REPAIR CANCER SYNDROME 2), OMIM:619096)

Official abbreviation MMRCS2
Name MISMATCH REPAIR CANCER SYNDROME 2
OMIM ID 619096
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MSH2
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:38:16 +00:00 (UTC)
Date last edited N/A

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